LANTHANIDE COMPOUNDS FOR LUMINESCENCE "TURN-ON" DETECTION

Abstract

The invention relates to luminescence-based compounds, compositions and methods for chemical sensing in solid state and solutions. More particularly, the invention includes “turn-on” lanthanide sensors that luminesce only in the presence of an organic compound (analyte) and are non-emissive in the absence of the organic compound (analyte).

Claims

1. A lanthanide-based, turn-on sensor, comprising: an organic analyte; and a lanthanide compound that luminesces in the presence of the organic analyte and does not luminesce in the absence of organic analyte, wherein the lanthanide-based, turn-on sensor is selected from the group consisting of a solid state, suspension, coating and solution.

2. The turn-on sensor of claim 1, wherein the organic analyte is selected from the group consisting of pharmaceutical contaminant, industrial chemical, biomarker, naturally occurring toxin, and combinations thereof.

3. The turn-on sensor of claim 1, wherein the organic analyte is selected from the group consisting of gossypol and polycyclic aromatic hydrocarbons.

4. The turn-on sensor of claim 1, wherein the lanthanide compound comprises a chemical element selected from the group consisting of lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium, and chemically similar elements scandium and yttrium, and combinations thereof.

5. The turn-on sensor of claim 1, wherein the lanthanide-based, turn-on sensor is in a form selected from the group consisting of metal-organic framework (MOF), complex, and simple salt.

6. The turn-on sensor of claim 1, wherein the lanthanide-based, turn-on sensor is in a form of a thin film.

7. The turn-on sensor of claim 1, wherein the lanthanide compound is selected from the group consisting of Ln-NH.sub.2-TPDC, Ln-NO.sub.2-TPDC, Ln-NH.sub.2-BDC and Ln-2NH.sub.2-BDC,and LnX.sub.3, where Ln represents Ln.sup.3+ cations and X represents an anion.

8. The turn-on sensor of claim 1, wherein the lanthanide compound is selected from the group consisting of Yb—NH.sub.2-TPDC, Yb—NO.sub.2-TPDC, Nd—NH.sub.2-TPDC, Nd—NO.sub.2-TPDC, Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC, and YbCl.sub.3.6H.sub.2O and NdCl.sub.3.6H.sub.2O.

9. A method of selectively sensing or detecting an organic analyte, comprising: preparing a lanthanide-based, turn-on sensor, comprising: providing a lanthanide compound that luminesces in the presence of the organic analyte and does not luminesce in the absence of organic analyte; providing a sample material; interacting the sample material and the lanthanide compound; and determining a presence or an absence of luminescence, wherein the presence of luminescence is indicative of a presence of the organic analyte in the sample material and the absence of luminescence is indicative of an absence of the organic analyte in the sample material, and wherein the lanthanide-based, turn-on sensor is selected from the group consisting of a solid state, suspension, coating and solution.

10. The method of claim 9, wherein the luminescence signal utilized for sensing lies in the spectral range of 700 nm-1600 nm.

11. The method of claim 9, wherein the providing the lanthanide compound step comprises reacting H.sub.2-NH.sub.2-TPDC solution and LnCl.sub.3.6H.sub.2O, wherein Ln represents a lanthanide element.

12. The method of claim 11, wherein Ln represents Yb or Nd.

13. The method of claim 9, wherein the providing the lanthanide compound step comprises reacting H.sub.2-NO.sub.2-TPDC solution and LnCl.sub.3.6H.sub.2O, wherein Ln represents a lanthanide element.

14. The method of claim 13 wherein Ln represents Yb or Nd.

15. The method of claim 9, wherein the providing the lanthanide compound step comprises reacting H.sub.2-NH.sub.2-BDC solution and LnCl.sub.3.6H.sub.2O, wherein Ln represents a lanthanide element.

16. The method of claim 15, wherein Ln represents Tb.

17. The method of claim 9, wherein the providing a lanthanide compound step comprises reacting H.sub.2-2NH.sub.2-BDC solution and LnCl.sub.3.6H.sub.2O, wherein Ln represents a lanthanide element.

18. The method of claim 17, wherein Ln represents Tb.

19. The method of claim 9, wherein the providing a lanthanide compound step comprises forming an LnCl.sub.3 solution, wherein Ln represents a lanthanide element.

20. The method of claim 19, wherein Ln represents Yb or Nd.

21. A gossypol sensor, comprising the luminescence-based, turn-on sensor of claim 1.

22. A polycyclic aromatic hydrocarbon sensor, comprising the luminescence-based, turn-on sensor of claim 1.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0025] The invention relates to luminescence-based elements, compounds, compositions and methods for selectively, chemical sensing or detecting organic compounds (analytes). The invention includes lanthanide-based, “turn-on” sensors that luminesce only in the presence of the organic compound (analyte) and are non-emissive in the absence of the organic compound (analyte). The lanthanide-based, turn-on sensors are in various forms or configurations, such as, but not limited to solid state, solution, suspension, coating, e.g., thin film. The turn-on sensor is useful for sensing or detecting a variety of organic compounds, such as, but not limited to, pharmaceutical contaminants, industrial chemicals, polycyclic aromatic hydrocarbons, biomarkers, and naturally occurring toxins.

[0026] In certain embodiments, the organic compound is gossypol (Gsp) having the chemical structure I:

##STR00001##

[0027] In certain other embodiments, the organic compound is selected from one or more polycyclic aromatic hydrocarbons (PAHs).

[0028] The luminescence-based compounds include lanthanide (Ln.sup.3+) compounds. As used herein and in the claims, the term “lanthanide compound(s)” and related terms refer to various substances containing a chemical element from the series of chemical elements that comprise the fifteen metallic chemical elements with atomic numbers 57-71 (in the Periodic Table of Elements), from lanthanum through lutetium, i.e., lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium, along with the chemically similar elements scandium and yttrium, (which are often collectively known as the rare earth elements), and combinations thereof.

[0029] The luminescence “turn-on” sensors are distinguishable from known luminescence “turn-off” sensors. For the “turn-off” sensors, the presence of analyte attenuates an existing luminescence intensity. The “turn-on” sensors have significantly less luminescence background and therefore, are potentially more sensitive and reliable than the “turn-off” sensors.

[0030] Luminescence-based methods, in general, are highly attractive for chemical sensing and exhibit advantages such as low limit of detection, high sensitivity, and fast response. An unusual and highly desirable feature of the luminescence “turn-on” sensors is that they are non-emissive in the absence of the analyte (organic compound), and only luminesce in the presence of the analyte (organic compound). Since the “turn-on” sensors have no background fluorescence, they have the advantage of being more sensitive and reliable than the alternative “turn-off” sensors, wherein the presence of analyte attenuates an existing luminescence intensity.

[0031] Another desirable feature of the “turn on” sensors according to the invention is that they are lanthanide-based sensors that are either insoluble, porous, solid-state materials or soluble lanthanide salts. This allows the “turn on” sensing devices to be fabricated in various, different configurations, such as metal-organic frameworks (MOFs), suspensions, coatings, thin films or solutions, as needed. A broad scope of lanthanide compounds, including MOFs, lanthanide complexes, and lanthanide salts, achieve optimized sensing performance, offering another degree of freedom for sensor optimization.

[0032] According to the invention, the luminescence “turn-on” sensors for the organic compounds use near infrared emitting lanthanide (Ln)-based materials including Ln MOFs and Ln salts. The photoluminescence of the Ln-based materials, selectively detect the organic compound (analyte) via a “turn-on” response from a completely non-emissive state in the absence of the organic compound. Common background substances that are present in practical samples of the organic compound do not interfere with the Ln photoluminescence signal. Further, the “turn-on” of the photoluminescence of the Ln-based materials is due to the “antenna” effect of the organic compound (analyte). Thus, the organic compound effectively sensitizes Ln photoluminescence. This sensing mechanism provides a facile, highly sensitive, fast-response detection of the organic compound (analyte). Thus, lanthanide-based materials serve as luminescent sensors for detection of a variety of organic compounds, such as, but not limited to, gossypol and a variety of PAHs.

[0033] The Ln-based materials according to the invention include MOFs such as Ln-NH.sub.2-TPDC and Ln-NO.sub.2-TPDC, wherein Ln represents Yb or Nd. The Ln-based materials also include MOFs such as Ln-NH.sub.2-BDC and Ln-2NH.sub.2-BDC, wherein Ln represents Tb. The Ln-based materials also include metal salts such as LnX.sub.3, wherein Ln represents Ln.sup.3+ cations and X represents an anion. In certain embodiments, Ln.sup.3+ represents Yb.sup.3+ or Nd.sup.3+, and X represents Cl. Furthermore, the metal salts are used to form solutions such as YbCl.sub.3.6H.sub.2O and NdCl.sub.3.6H.sub.2O.

[0034] In accordance with the invention, Ln-based MOFs are synthesized by reacting a solution of 3,3″-diamino-1,1′:4′,1″-terphenyl-4,4″-dicarboxylic acid (H.sub.2-NH.sub.2-TPDC) or a solution of 2″-nitro-1,1′:4′,1″-terphenyl-4,4″-dicarboxylic acid (H.sub.2-NO.sub.2-TPDC), and a solution of LnX.sub.3.6H.sub.2O with an acid, such as, 2,6-difluorobenzoic acid in solvent. In certain embodiments, the Ln materials Ln-NH.sub.2TPDC and Ln-NO.sub.2TPDC of the invention are prepared by reacting a dimethylformamide (DMF) solution of 3,3″-diamino-1,1′:4′,1″-terphenyl-4,4″-dicarboxylic acid (H.sub.2-NH.sub.2-TPDC) (e.g., 1.5 mL, 0.05 M) or a DMF solution of 2″-nitro-1,1′:4′1″-terphenyl-4,4″-dicarboxylic acid (H.sub.2-NO.sub.2-TPDC) (e.g., 1.5 mL, 0.05 M), and a DMF solution of LnCl.sub.3.6H.sub.2O (e.g., 0.75 mL, 0.05 M) with an acid, such as, 2,6-difluorobenzoic acid in DMF (e.g., 0.75 mL, 1 M), water, such as, nanopure H.sub.2O (e.g., 0.15 mL) and solvent, such as, concentrated hydrochloric acid/DMF (0.2 mL), in a capped vial placed in an isothermal oven (e.g., 120° C.) for a period of time (e.g., about 14 hours). The vial is then removed from the oven and cooled down naturally to room temperature. Ln-NH.sub.2-TPDC crystals or Ln-NO.sub.2-TPDC crystals, respectively, are collected after centrifugation and washed with fresh solvent, e.g., DMF (e.g., 3 times using 2 mL each time).

[0035] The Ln-based materials are prepared for sensing the organic compound (analyte) by preparing a slurry containing the synthesized Ln-based material and solvent, and grinding with a mortar and pestle to reduce the size of the Ln-based crystals. The presence of a solvent contributes to the Ln-based material retaining crystallinity during the grinding processing. The ground sample is then solvent exchanged, in a vial in accordance with conventional apparatus and techniques. In certain embodiments, the Ln-based MOF materials Ln-NH.sub.2TPDC or Ln-NO.sub.2TPDC are prepared for sensing the organic compound (analyte) by preparing a slurry containing the synthesized Ln-NH.sub.2-TPDC (e.g., approx. 45 mg) or Ln-NO.sub.2TPDC (e.g., approx. 45 mg), and solvent, such as DMF, (e.g., 0.5 mL), and grinding with a mortar and pestle (e.g., for 20 min) to reduce the size of the Ln-NH.sub.2-TPDC crystals or Ln-NO.sub.2-TPDC crystals. The presence of a solvent contributes to the Ln-NH.sub.2-TPDC or Ln-NO.sub.2-TPDC retaining crystallinity during the grinding processing. The ground sample is then solvent exchanged, e.g., with dichloromethane and n-pentane, in a vial in accordance with conventional apparatus and techniques. For example, to perform solvent exchange, the vial is loaded in a centrifuge tube as secondary container and centrifuged (e.g., at 3000 rpm for 3 min) to form a sample pellet at the bottom the vial. Most of supernatant is removed, with enough solvent remaining to ensure the MOF sample is submerged. The vial is replenished with fresh solvent, and the MOF sample is re-dispersed (e.g., via vortexing). The solvent exchange procedure is typically performed multiple times. In certain embodiments, the solvent exchange is performed every 20 min, with dichloromethane (4 mL each time) for five times and then n-pentane (4 mL each time) for five times. Following the last solvent exchange cycle, the solvent is removed, followed by drying. The Ln-NH.sub.2-TPDC or Ln-NO.sub.2-TPDC is then ready for use as a “turn on” sensor to sense and detect the organic compounds.

[0036] For sensing or detecting, a dispersion of an Ln-based material (e.g., MOF suspension or LnX.sub.3/Ln complex solution) is prepared and a solution of an organic compound (analyte) is prepared. The Ln-based material dispersion and the organic compound solution are combined to form a mixture, wherein the luminescence of the mixture is indicative of the organic compound interacting with the lanthanide compound. In certain embodiments, the Ln-based material Ln-NH.sub.2-TPDC or Ln-NO.sub.2-TPDC is prepared. The Ln-NH.sub.2-TPDC (e.g., 2.5 mg) or Ln-NO.sub.2-TPDC (e.g., 2.5 mg) is dispersed with acetone (e.g., 2 mL). A solution of the organic compound is prepared, for example, organic compound/acetone solution, and added to the MOF suspension to form a mixture. Emission spectra of the mixture is then conducted. In certain embodiments, the emission spectra is obtained using 485 nm excitation wavelength.

[0037] In certain embodiments, a solution of an Ln-based material is prepared by dissolving a commercially available Ln salt in a solvent, and a solution of an organic compound (analyte) is prepared by dissolving the organic compound in a solvent. The Ln salt solution and the organic compound solution are combined to form a mixture, wherein the luminescence of the mixture is indicative of the organic compound interacting with the Ln salt. In certain embodiments, YbCl.sub.3.6H.sub.2O (e.g., 2 mg) or NdCl.sub.3.6H.sub.2O (e.g., 2 mg) is dissolved with DMF (e.g., 2 mL). A solution of the organic compound is prepared, for example, organic compound/acetone solution, and added to the Ln salt solution to form a mixture. Emission spectra of the mixture is then conducted. In certain embodiments, the emission spectra are obtained using 400 nm excitation wavelength.

[0038] The amount or concentration of organic compound (analyte) added to the Ln sensor varies. In certain embodiments, the sensitivity of the sensor depends on the amount or concentration of the organic compound (analyte). In certain embodiments, the concentration of organic compound in a sensor solution is from 0.5 to 100 μg/mL. High sensitivity of the sensor solution (e.g, YbCl.sub.3.6H.sub.2O or NdCl.sub.3.6H.sub.2O) is achieved when the concentration of organic compound (analyte) in the sensor solution is from 0.5 to 10 μg/mL.

[0039] In certain embodiments, the lanthanide-based “turn-on” sensor includes Yb.sup.3+ or Nd.sup.3+ photoluminescence of a ytterbium (Yb) or neodymium (Nd) MOF, Yb—NH.sub.2TPDC or Nd—NH.sub.2TPDC, or Yb or Nd salt (YbCl.sub.3.6H.sub.2O or NdCl.sub.3.6H.sub.2O), that selectively detects an organic compound (analyte), such as, but not limited to, gossypol (e.g., with a limit of detection of 25 μg/mL) via a “turn-on” response from a completely non-emissive state in the absence of the organic compound (analyte), e.g., gossypol. A variety of background substances that are present in practical samples of gossypol, such as refined cotton-seed oil, palmitic acid, linoleic acid and α-tocopherol, do not interfere with the Yb.sup.3+ or Nd.sup.3+ photoluminescence signal. Further, the “turn-on” of Yb—NH.sub.2TPDC or Nd—NH.sub.2TPDC photoluminescence is due to the “antenna” effect of gossypol and therefore, gossypol effectively sensitizes Yb.sup.3+ or Nd.sup.3+ photoluminescence. This sensing mechanism provides a facile, highly sensitive, fast-response detection of gossypol using YbCl.sub.3.6H.sub.2O or NdCl.sub.3.6H.sub.2O solutions.

[0040] Two salient features of gossypol make it an effective antenna molecule for sensitizing Ln.sup.3+ photoluminescence (PL): (i) gossypol is a yellow pigment with strong absorption of visible light, while most organic linkers can only effectively absorb UV light; and (ii) the multiple hydroxyl substituents and aldehyde groups of the two naphthalene cores of gossypol are potential polydentate binding sites for Ln.sup.3+. Furthermore, aromatic aldehyde groups, like those in gossypol, react with aromatic amine-functionalized MOF linkers to form Schiff base and effectively red-shift the sensitization wavelengths of the integral antenna in Ln materials. These two scenarios allow for the sensitization of Ln.sup.3+ PL at longer wavelengths in the presence of gossypol.

[0041] In certain embodiments of the invention, a MOF analogue of a Ln.sup.3+ fcu MOF platform using 3,3″-diamino-1,1′:4′,1″-terphenyl-4,4″-dicarboxylic acid (H.sub.2-NH.sub.2TPDC) and YbCl.sub.3.6H.sub.2O, denoted as Yb—NH.sub.2TPDC, is synthesized. The Yb.sup.3+ centered near infrared (NIR) emission is advantageous for molecular sensing, as it avoids overlapping with sample fluorescence in the visible spectrum. The Yb—NH.sub.2TPDC with fcu topology has a crystal structure (as confirmed by single crystal X-ray diffraction).

[0042] In certain embodiments, the Ln-based materials (e.g., Ln-NH.sub.2BDC and Ln-2NH.sub.2BDC), e.g., terbium-based materials, are used for sensing PAHs, e.g., OH-Py carcinogenic PAHs biomarkers, in a urine specimen or sample derived from a human, e.g., patient. Amino and diamino functionalized MOFs are prepared by reacting 2-amino-1,4-benzenedicarboxylic acid (H.sub.2-NH.sub.2-BDC) or 2,5-diamino-1,4-benzenedicarboxylic acid (H.sub.2-2NH.sub.2-BDC) with TbCl.sub.3.6H.sub.2O. For example, the reaction is conducted in a mixture of solvent, such as, dimethylformamide (DMF), water and nitric acid solution at 120° C. to yield cubic crystals denoted as {[(Me.sub.2NH.sub.2).sub.2[Tb.sub.6(C.sub.8H.sub.5NO.sub.2).sub.6.6H.sub.2O].12DMF}.sub.n(Tb—NH.sub.2-BDC) or {[(Me.sub.2NH.sub.2).sub.2[Tb.sub.6(C.sub.8H.sub.6N.sub.2O.sub.2).sub.6.6H.sub.2O].10DMF}.sub.n Tb-2NH.sub.2-BDC, respectively.

[0043] The “turn-on” sensing ability of activated Tb—NH.sub.2-BDC and Tb-.sub.2NH.sub.2-BDC towards OH-Py shows a fast response of OH-Py in presence of both MOFs. Selective fluorescence “turn-on” of activated Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC towards other urine components such as uric acid, hippuric acid (Hipp), creatine, creatinine, urea, glucose, NH4Cl, NaCl and KCl under the same condition show that both MOFs exhibit highly selective turn-on response towards OH-Py, whereas negligible to moderate response for other urine components under the same conditions. This is because the other urine analytes cannot absorb visible light or modulate the absorption of Tb-NH.sub.2-BDC and Tb-2NH.sub.2-BDC. Therefore, the other interfering urine components cannot excite under 375 nm and are missing the spectral overlap. Thus, both Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC are efficient “turn-on” sensors for OH-Py.

[0044] In accordance with the invention, H.sub.2-NH.sub.2-TPDC solution is reacted with LnCl.sub.3.6H.sub.2O to form sensing material Ln-NH.sub.2-TPDC, wherein Ln represents a lanthanide element or Ln represents ytterbium or neodymium; H.sub.2-NO.sub.2-TPDC solution is reacted with LnCl.sub.3-6H.sub.2O to form sensing material Ln-NO.sub.2-TPDC, wherein Ln represents a lanthanide element, or Ln represents ytterbium or neodymium; H.sub.2-NH.sub.2-BDC solution is reacted with LnCl.sub.3.6H.sub.2O to form sensing material Ln-NH.sub.2-BDC, wherein Ln represents a lanthanide element or Ln represents terbium; and H.sub.2-2NH.sub.2-BDC solution is reacted with LnCl.sub.3.6H.sub.2O, to form sensing material Ln-2NH.sub.2-BDC, wherein Ln represents a lanthanide element or Ln represents terbium.

[0045] In accordance with the invention, the Ln-based turn-on sensors are used to selectively sense or detect an organic compound (analyte). In certain embodiments, a sample or specimen, e.g., solid, solution or suspension, is provided that potentially contains the organic compound. The Ln-based turn-on sensor is utilized to determine whether the sample or specimen contains the organic compound, e.g., gossypol or polycyclic aromatic hydrocarbon. The Ln-based material of the invention is prepared and placed in contact, or interacted, with the sample or specimen. Since the Ln-based material luminesces in the presence of the organic compound and does not luminesce in the absence of the organic compound, the sample or specimen is assessed for luminescence. The presence of luminescence is indicative of the presence of the organic compound in the sample or specimen, and the absence of luminescence is indicative of an absence of the organic analyte in the sample or specimen.

[0046] While specific embodiments of the invention have been described in detail, it will be appreciated by those skilled in the art that various modifications and alternatives to those details could be developed in light of the overall teachings of the disclosure. Accordingly, the particular arrangements disclosed are meant to be illustrative only and not limiting as to the scope of the invention which is to be given the full breadth of the claims appended and any and all equivalents thereof.

EXAMPLES

[0047] In the following examples, all purchased chemicals were used without further purification except where otherwise noted. Refined cottonseed oil, gossypol, palmitic acid, linoleic acid, α-tocopherol were purchased from Sigma-Aldrich. Nanopure water (18.1 MΩ) was obtained from a Barnstead Diamond™ water purification system. X-ray powder diffraction patterns were collected using a Bruker AXS D8 Discover powder diffractometer at 40 kV, 40 mA for Cu Kα, (λ=1.5406 Å) from 3 to 45° at a step size of 0.02°. The data were analyzed using the EVA program from the Bruker Powder Analysis Software package. The simulated powder patterns were calculated using Mercury 3.8 and CIF files. Single crystal X-ray diffraction experiments were performed on a Bruker X8 Prospector Ultra diffractometer equipped with an Apex II CCD detector and an IμS micro-focus Cu Kα X-ray source (λ=1.54178 Å). Data were collected at 230 K under N.sub.2 flow and processed using the Bruker APEX II software package and refined with Olex2 program. .sup.1H NMR spectra were collected using Bruker Avance III 300 MHz spectrometers. Chemical shifts are in parts per million (ppm) using the residual solvent peak (DMSO-d.sub.6) as references. Thermogravimetric analyses (TGA) were performed using a TGA Q500 thermal analysis system under a N.sub.2 atmosphere from room temperature to 650° C. at a ramping rate of 5° C. /min. Solution UV—Vis absorption spectra were collected using an Agilent 8453 UV—Vis spectrometer equipped with deuterium and tungsten lamps. Photoluminescence measurements were collected using a Horiba Jobin-Yvon NanoLog spectrofluorometer with a 450 W xenon source, double excitation monochromators, and a Symphony II InGaAs array detector. Excitation gratings were blazed at 330 nm with 1200 grooves/mm and emission gratings blazed at 780 nm with 100 grooves/mm. All measurements were obtained with an 830 nm long-pass filter at ambient temperature.

Example 1

Synthesis of Yb—NH.SUB.2.TPDC[Yb.SUB.6.(OH).SUB.8.(C.SUB.20.H.SUB.14.N.SUB.2.O.SUB.4.).SUB.6.(H.SUB.2.O).SUB.6].2.(C.SUB.2.H.SUB.8.N).17DMF.6H.SUB.2.O

[0048] Stock solutions of H.sub.2-NH.sub.2-TPDC (0.05 M) and YbCl.sub.3.6H.sub.2O (0.05 M) and 2,6- difluorobenzoic acid (1 M) in DMF were prepared. A mixture of concentrated hydrochloric acid/DMF (1/2.3 v/v) was prepared. To a 20 mL Pyrex vial was added H.sub.2-NH.sub.2-TPDC solution (1.5 mL, 0.05 M), YbCl.sub.3.6H.sub.2O (0.75 mL, 0.05 M), 2,6-difluorobenzoic acid (0.75 mL, 1 M), nanopure H.sub.2O (0.15 mL) and concentrated hydrochloric acid/DMF (0.2 mL) sequentially. The vial was tightly capped and heated in a 120° C. isothermal oven for 14 hours. The vial was then removed from oven and cooled down naturally to room temperature. Crystals were collected after centrifugation and washed with fresh DMF (3×, 2 mL each time). Yield: 15 mg. Anal. calcd. (%): C, 43.76; H, 5.27; N, 9.04; Found (%): C, 43.09; H, 4.68; N, 9.32.

[0049] The experimental PXRD pattern of as-synthesized Yb—NH.sub.2-TPDC and the simulated PXRD pattern of Yb—NH.sub.2-TPDC based on its crystal structure were produced. The experimental power X-ray diffraction (PXRD) pattern of the Yb—NH.sub.2TPDC bulk sample closely matched the simulated PXRD pattern of Yb—NH.sub.2TPDC, indicating high phase purity.

.SUP.1.H NMR of Digested Yb—NH.SUB.2.-TPDC Sample

[0050] Approximately 3 mg of the as-synthesized Yb—NH.sub.2-TPDC was dried under argon flow and then dissolved with ˜500 μL of DMSO-d.sub.6 and 30 μL of DCl/D.sub.2O. An .sup.1H NMR spectrum was collected on the sample solution, which showed two singlets at 2.48 ppm, and 8.15 ppm corresponding to protons from (CH.sub.3).sub.2NH.sup.2+.

Sample Activation and N.SUB.2 .Gas Adsorption Experiment of Yb—NH.SUB.2.TPDC

[0051] Two batches of as-synthesized Yb—NH.sub.2TPDC were prepared (vide supra) and combined in a 20 mL Pyrex vial after being thoroughly washed with DMF. Solvent exchange was performed with dichloromethane and then n-pentane. To perform solvent exchange, most of existing solvent in the sample vial was removed using a glass pipette with enough solvent remaining to submerge the MOF sample. The vial was then replenished with fresh solvent. This solvent exchange procedure was performed every 20 min, with dichloromethane (6 mL each time) for the first 5 cycles and then n-pentane (12 mL each time) for another 5 cycles. After the last solvent exchange cycle with n-pentane, the solvent was removed by pipetting followed by drying under argon flow. The MOF sample was then evacuated on a Micromeritics Smart VacPrep at room temperature for 21 hours to obtain 29.4 mg of activated sample. N.sub.2 isotherm of MOF samples were collected at 77K on a Micromeritics 3Flex instrument.

[0052] Yb—NH.sub.2TPDC was successfully activated under vacuum at room temperature without losing crystallinity after stepwise solvent exchange with dichloromethane and n-pentane. N.sub.2 adsorption analysis of activated Yb—NH.sub.2TPDC at 77K yielded a type I isotherm with a Brunauer-Emmett-Teller (BET) surface area of 2370 m2/g.

Excitation-Emission Maps of Yb—NH.SUB.2.-TPDC Samples

[0053] Excitation-emission maps of Yb—NH.sub.2-TPDC samples with and without gossypol were measured using an integration sphere on solid MOF samples stored under acetone in quartz capillary tubes. The excitation wavelength was scanned from 300 to 700 nm in 5 nm increments, and the emission was detected between 820 to 1580 nm with 1.5 nm increments. Slit widths were set at 10 nm for both excitation and emission. An integration time of 10 s was used for each emission spectrum.

[0054] The Yb—NH.sub.2-TPDC samples were prepared using the following procedure. Two samples each containing 2.5 mg of activated Yb—NH.sub.2-TPDC were incubated, respectively, with acetone (1 mL) and gossypol/acetone solution (0.1 mg/mL, 1 mL) in 1.5 mL centrifuge tubes at 20° C. for 44 hours using a thermal mixer at 1000 rpm. After the incubation time, the MOF crystals were centrifuged and transferred to custom-made quartz tubes with 0.5 mL of the incubation solvent or solution. The quartz tubes were sealed with parafilm to prevent solvent evaporation.

Sensing Experiments Using Yb—NH.SUB.2.-TPDC

[0055] A slurry containing three batches of as-synthesized Yb—NH.sub.2-TPDC (approx. 45 mg) and 0.5 mL of DMF was ground with a mortar and pestle for 20 min to reduce the size of Yb—NH.sub.2-TPDC crystals. Grinding without DMF will cause Yb—NH.sub.2-TPDC to lose crystallinity. The ground sample was then solvent exchanged with dichloromethane and n-pentane in a 5 mL sample vial. To perform solvent exchange, the sample vial was loaded in a 50 mL centrifuge tube as secondary container and centrifuged at 3000 rpm for 3 min to form a sample pellet at the bottom the vial. Most of supernatant was removed using a glass pipette with enough solvent left to ensure the MOF sample was submerged. After the vial was replenished with fresh solvent, MOF sample was re-dispersed via vortexing. This solvent exchange procedure was performed every 20 min, with dichloromethane (4 mL each time) for 5 times and then n-pentane (4 mL each time) for 5 times. After the last solvent exchange cycle with n-pentane, the solvent was removed by pipetting followed by drying under argon flow. After evacuating under Schlenk vacuum for 1 hour, the Yb—NH.sub.2-TPDC sample was ready for sensing experiments.

[0056] For gossypol sensing experiments, 2.5 mg of Yb—NH.sub.2-TPDC was dispersed with 2 mL of acetone in a standard fluorescence macro cuvette equipped with a PTFE stopper (Fireflysci type 21 macro cuvette, light path: 10 mm×10 mm). Approx. 1 mL of gossypol/acetone solution (0 μg/mL, 25 μg/mL, 50 μg/mL, 75 μg/mL, 100 μg/mL) was then added to the MOF suspension. The cuvette was tightly capped, mounted on top of a thermomixer (Eppendorf Thermomixer R Mixer) using a custom-made sample holder and incubated at room temperature with 500 rpm mixing frequency. Emission spectra of each sample was followed over 300 min. The cuvette was vigorously shaken with hand and emission spectra were immediately collected. The emission spectra were obtained using 485 nm excitation wavelength. The emission was detected between 820 to 1580 nm with 1.5 nm increments. Slit widths were set at 10 nm for both excitation and emission. An integration time of 1 s was used for each emission spectrum.

[0057] For gossypol sensing interference experiments, 1 mL of 2.5 mg/mL Yb—NH2-TPDC in acetone was mixed with 1 mL of acetone (blank) or gossypol/acetone solution (100 μg/mL) and 1 mL of interferant acetone solution, including: cotton-seed oil (100 mg/mL), palmitic acid (1 mg/mL), linoleic acid (1 mg/mL) and α-tocopherol (1 mg/mL). The mixture was incubated on top of a thermomixer (Eppendorf Thermomixer R Mixer) in a 15 mL centrifuge tube at room temperature for 300 min with 500 rpm mixing frequency and then transferred to a standard fluorescence macro cuvette equipped with a PTFE stopper (Fireflysci type 21 macro cuvette, light path: 10 mm×10 mm). The cuvette was vigorously shaken with hand and emission spectra were immediately collected. The emission spectra were obtained using 485 nm excitation wavelength. The emission was detected between 820 to 1580 nm with 1.5 nm increments. Slit widths were set at 10 nm for both excitation and emission. An integration time of 1 s was used for each emission spectrum.

Synthesis of Yb—NO.SUB.2.TPDC

[0058] Stock solutions of H.sub.2-NO.sub.2-TPDC (0.05 M) and YbCl.sub.3.6H.sub.2O (0.05 M) and 2,6- difluorobenzoic acid (1 M) in DMF were prepared. To a 4 mL Pyrex vial equipped with a PTFE cap was added H.sub.2-NO.sub.2TPDC solution (0.3 mL, 0.05 M), YbCl.sub.3.6H.sub.2O (0.15 mL, 0.05 M), 2,6-difluorobenzoic acid (0.25 mL, 1 M) sequentially. The vial was tightly capped and heated in a 100° C. isothermal oven for 40 hours. The vial was then removed from oven and cooled down naturally to room temperature. Crystals were collected after centrifugation and washed with fresh DMF (3×, 1 mL each time). Yield: 2.3 mg.

[0059] The experimental PXRD pattern of as-synthesized Yb—NO2-TPDC and the simulated PXRD pattern of Yb—NH.sub.2-TPDC based on its crystal structure were produced. The close match between the two PXRD patterns indicates Yb—NO.sub.2-TPDC is an isoreticular analogue of Yb—NH.sub.2-TPDC.

Excitation-Emission Maps of Yb—NO.SUB.2.-TPDC Samples

[0060] Excitation-Emission maps of Yb—NO.sub.2-TPDC samples with and without gossypol were measured using an integration sphere on solid MOF samples stored under acetone in quartz capillary tubes. The excitation wavelength was scanned from 300 to 700 nm in 5 nm increments, and the emission was detected between 820 to 1580 nm with 1.5 nm increments. Slit widths were set at 10 nm for both excitation and emission. An integration time of 10 s was used for each emission spectrum.

[0061] The Yb—NO.sub.2-TPDC samples were prepared using the procedure as follows. Two samples containing 6 mg of as-synthesized Yb—NO.sub.2-TPDC were first washed with acetone (4 times, 1 mL each time), and then incubated respectively with acetone (1 mL) and gossypol/acetone solution (0.1 mg/mL, 1 mL) in 1.5 mL centrifuge tubes at 20° C. for 44 hours using a thermomixer (Eppendorf Thermomixer R Mixer) with 1000 rpm mixing frequency. After the incubation time, the MOF crystals were centrifuged and transferred to quartz tubes with 0.5 mL of the incubation solvent or solution. The quartz tubes were sealed with parafilm to prevent solvent evaporation. Excitation-Emission maps were collected when all of the MOF crystals settled to the bottom of the quartz tubes.

Liquid Chromatography-Mass Spectrometry (LC-MS) Experiments

[0062] Yb—NH.sub.2-TPDC (5.7 mg) was incubated in gossypol/acetone solution (0.1 mg/mL, 2 mL) at 20° C. for 44 h on a thermomixer (Eppendorf Thermomixer R Mixer) at room temperature with 500 rpm mixing frequency. After incubation, the MOF crystals were washed with ethanol (3 times, 3 mL each time). To the washed MOF crystals were then added NaBH4/EtOH solution (10 mg/mL,3 mL) in a Pyrex vial. The mixture was allowed to react at room temperature for 18 hrs. The solid in the mixture was separated via centrifugation and then washed with fresh EtOH (3 times, 1 mL each time). To the solid was then added aqueous HCl solution (1 M, 1 mL). After sonicating for 5 min, the mixture was centrifuged,and supernatant removed. The precipitate was then dissolved in MeOH (1 mL). The solution was then submitted to LC-MS.

[0063] In ESI+ mode, the [M+H]+ peak for NH.sub.2-TPDC linker (m/z=349) was observed along with additional peaks. However, no peaks corresponding to the two possible reduced Schiff base products were identified.

[0064] Yb—NH.sub.2-TPDC MOF (2.5 mg) was incubated with gossypol acetone solution (0.1 mg/mL, 1 mL) at room temperature for 42 hrs. The supernatant was collected and examined with LC-MS using ESI− mode. Mass spectrometry data indicate that gossypol molecules in solution were intact after incubation with MOF in acetone for 42 hours.

[0065] Mass spectrum (ESI−) of gossypol solution after incubating with MOF Yb—NH.sub.2-TPDC showed the three peaks with m/z=517, m/z=557, m/z=597 corresponding, respectively, to [M−H]—, [M.sup.+acetone-H.sub.2O—H]— and [M.sup.+2(acetone-H.sub.2O)—H]—.

Excitation-Emission Map of YbCl.SUB.3..6H.SUB.2.O Sample in the Presence of Gossypol

[0066] Excitation-Emission maps of YbCl.sub.3 in the presence of gossypol were measured on a solution sample in a macro cuvette. The excitation wavelength was scanned from 300 to 700 nm in 10 nm increments, and the emission was detected between 820 to 1580 nm with 1.5 nm increments. Slit widths were set at 10 nm for both excitation and emission. An integration time of 1 s was used for each emission spectrum.

[0067] The sample was prepared using the following procedure. The YbCl.sub.3.6H.sub.2O (2.3 mg) was dissolved in DMF (2 mL) in a standard fluorescence macro cuvette equipped with a PTFE stopper (Fireflysci type 21 macro cuvette, light path: 10 mm×10 mm). Gossypol/acetone solution (0.005 mg/mL, 1 mL) was added to the cuvette. The mixture was incubated at room temperature for 5 minutes before excitation-emission map was collected.

Gossypol Sensing Experiments Using YbCl.SUB.3

[0068] A stock solution of 1 mg/mL YbCl.sub.3.6H.sub.2O in DMF was prepared by dissolving YbCl.sub.3.6H.sub.2O (30.7 mg) in DMF (30.7 mL) in a 40 mL Pyrex vial. In each sensing experiment, 2 mL of the YbCl.sub.3.6H.sub.2O solution (1 mg/mL) was added in a standard fluorescence macro cuvette equipped with a PTFE stopper (Fireflysci type 21 macro cuvette, light path: 10 mm×10 mm). 1 mL of gossypol/acetone solution (0 μg/mL, 0.5 μg/mL, 1 μg/mL, 3 μg/mL, 5 μg/mL, 7 μg/mL, 10 μg/mL, 25 μg/mL, 50 μg/mL) was then added to the cuvette. The cuvette was capped and incubated at room temperature for 5 min on top of a thermomixer (Eppendorf Thermomixer R Mixer) with 500 rpm mixing frequency before emission spectra were collected. The emission spectra were obtained using 400 nm excitation wavelength. The emission was detected between 820 to 1580 nm with 1.5 nm increments. Slit widths were set at 10 nm for both excitation and emission. An integration time of 1 s was used for each emission spectrum.

[0069] Emission intensities at 976 nm of YbCl.sub.3 solution in the presence of various gossypol concentrations were determined. The sensor solution had the highest sensitivity when gossypol concentration was between 0.5 and 10 μg/mL. To quantify gossypol concentrations between 0.5 and 10 μg/mL, a linear calibration curve was sufficient; emission intensities of YbCl.sub.3 solution and gossypol concentrations in the range of 0.5-50 μg/mL were fit by an exponential curve.

Gossypol Sensing Experiments Using NdCl.SUB.3

[0070] A stock solution of 1 mg/mL NdCl.sub.3.6H.sub.2O in DMF was prepared by dissolving NdCl.sub.3.6H.sub.2O (23.1 mg) in DMF (23.1 mL) in a 40 mL Pyrex vial. In each sensing experiment, 2 mL of the NdCl.sub.3.6H.sub.2O solution (1 mg/mL) was added in a standard fluorescence macro cuvette equipped with a PTFE stopper (Fireflysci type 21 macro cuvette, light path: 10 mm×10 mm). 1 mL of gossypol/acetone solution (0 μg/mL, 1μg/mL, 3 μg/mL, 5 μg/mL, 7 μg/mL, 10 μg/mL, 25 μg/mL, 50 μg/mL, 75 μg/mL, 100 μg/mL) was then added to the cuvette. The cuvette was capped and incubated at room temperature for 5 min on top of a thermomixer at 500 rpm before emission spectra were collected. The cuvette was capped and incubated at room temperature for 5 min on top of a thermomixer (Eppendorf Thermomixer R Mixer) with 500 rpm mixing frequency before emission spectra were collected. The emission spectra were obtained using 400 nm excitation wavelength. The emission was detected between 820 to 1580 nm with 1.5 nm increments. Slit widths were set at 10 nm for both excitation and emission. An integration time of 1 s was used for each emission spectrum.

[0071] Emission intensities at 1056 nm of NdCl.sub.3 solution in the presence of various gossypol concentrations were determined. The sensor solution had the highest sensitivity when gossypol concentration was between 0.5 and 10 μg/mL. To quantify gossypol concentrations between 0.5 and 10 μg/mL, a linear calibration curve was sufficient; emission intensities of YbCl.sub.3 solution and gossypol in the range of 0.5-100 μg/mL were fit by an exponential curve.

Discussion

[0072] The MOF analogue of the well-established Ln.sup.3+ fcu MOF platform was synthesized using 3,3″-diamino-1,1′:4′,1″-terphenyl-4,4″-dicarboxylic acid (H.sub.2-NH.sub.2-TPDC) and YbCl.sub.3.6H.sub.2O, denoted as Yb—NH.sub.2-TPDC. The Yb.sup.3+-centered near infrared (NIR) emission is advantageous for molecular sensing, as it does not overlap with sample fluorescence in the visible spectrum. The anticipated crystal structure of Yb—NH.sub.2-TPDC with fcu topology was confirmed by single crystal X-ray diffraction data. The experimental powder X-ray diffraction (PXRD) pattern of the bulk sample closely matched the simulated PXRD pattern of Yb—NH.sub.2-TPDC, indicating high phase purity. The [Yb.sub.6(OH).sub.8(COO).sub.12].sup.2− secondary building units (SBUs) make Yb—NH.sub.2-TPDC a negatively charged framework. The charge balancing cation, dimethylammonium, was observed from .sup.1H NMR of the digested sample. With equilateral triangular pore apertures that measure 13.5 Å in altitude, when accounting for Van der Waals radii, Yb—NH.sub.2-TPDC should allow entry of gossypol, which measures approximately 10.4 Å×10.7 Å×16.9 Å. A coordinating oxygen atom, likely either from a water or dimethyl formamide (DMF) molecule, was observed near each Yb.sup.3+ ion of the BU, indicating a possible coordination site for gossypol molecules. Thermogravimetric analysis showed a steep weight loss below 120° C. corresponding to evaporation of solvent guests and a more gradual weight loss after 120° C. The lack of a well-defined plateau signifies poor thermal stability above 120° C. Yb—NH.sub.2-TPDC was successfully activated under vacuum at room temperature without losing crystallinity after stepwise solvent exchange with dichloromethane and n-pentane. The N.sub.2 adsorption analysis at 77K of activated sample yielded a type I isotherm from which the Brunauer-Emmett-Teller (BET) surface area of 2370 m.sup.2/g was determined.

[0073] In the absence of gossypol, a solid Yb—NH.sub.2-TPDC sample under acetone, when excited between 300-475 nm, exhibited the characteristic Yb.sup.3+ NIR emission band at 940-1060 nm corresponding to .sup.2F.sub.5/2.fwdarw..sup.2F.sub.7/2 transition of Yb.sup.3+. Since Yb.sup.3+ does not have electronic levels that can be excited with ultraviolet or visible light, the Yb.sup.3+ PL of Yb—NH.sub.2-TPDC must be due to the “antenna effect” of the NH.sub.2-TPDC linker. Notably, the excitation band of Yb—NH.sub.2-TPDC (300-475 nm) was red-shifted in comparison to the UV-vis absorption spectrum of H.sub.2-NH.sub.2-TPDC in solution, which showed two bands centered at 300 nm and 360 nm and no significant absorption at wavelengths above 410 nm. Similar effects were observed in a different MOF. This large discrepancy may be due to confinement effects, where the MOF architecture forces molecules to adopt different conformations than those in solution. Intriguingly, incubating Yb—NH.sub.2-TPDC with gossypol led to a red-shift of the long wavelength edge of the excitation band of Yb.sup.3+ PL from 475 nm as observed in the blank sample to 550 nm. Compared to the blank sample, a decrease in Yb.sup.3+ PL intensity in the presence of gossypol was also noted when Yb—NH.sub.2-TPDC was excited between 340 and 400 nm. This was ascribed to the attenuation of incident light caused by the strong light absorption of gossypol in solution in this range. These results indicate that under excitation between 475 nm and 550 nm, the Yb.sup.3+ PL of Yb—NH.sub.2-TPDC can be switched on from a complete non-emissive state in response to the presence of gossypol.

[0074] The kinetics of Yb.sup.3+ PL of Yb—NH.sub.2-TPDC in response to gossypol was then evaluated. Specifically, 1 mL of gossypol/acetone solution (25 μg/mL, 50 μg/mL, 75 μg/mL, 100 μg/mL) was added to 2 mL of acetone suspension containing 2.5 mg of Yb—NH.sub.2-TPDC powder in a standard macro fluorescence cuvette. Yb.sup.3+ PL was immediately monitored for 300 min under 485 nm excitation light. Upon addition of gossypol, Yb.sup.3+ emission gradually increased over 300 min. The slow increase of PL intensity was likely due to the hindered diffusion of the bulky gossypol within Yb—NH.sub.2-TPDC. With an equal amount of incubation time, stronger Yb.sup.3+PL intensity correlates with higher gossypol concentration in the 25-100 μg/mL range. At 300 min, Yb.sup.3+ PL intensity follows a linear dependence with gossypol concentration between 25 μg/mL and 100 μg/mL, and therefore is suitable for quantification of gossypol in this concentration range. No appreciable Yb.sup.3+ emission was observed in the absence of gossypol. The limit of detection was determined to be 25 μg/mL (˜32 ppm in acetone solution) with a S/N of 7. No reliable Yb.sup.3+ emission was detected when solutions of lower concentrations were tested. The actual minimum detectable gossypol concentration was 8.3 μg/mL (˜11 ppm in acetone solution), because the 1 mL of 25 μg/mL gossypol solution was diluted into 3 mL in cuvette. Despite the relatively slow response, Yb—NH.sub.2-TPDC is an effective sensor for practical detection and quantification of gossypol in terms of its limit of detection.

[0075] Interference from background molecules present in realistic samples, such as cottonseed oil and cotton meals, may hamper gossypol detection and quantification. To evaluate the selectivity of Yb—NH.sub.2-TPDC as a sensor for gossypol, it was further evaluated whether Yb.sup.3+ PL excited at 485 nm can be turned on by substances commonly present in the context of gossypol detection.

[0076] Refined cottonseed oil solution (100 mg/mL), palmitic acid solution (1 mg/mL), linoleic acid solution (1 mg/mL), and α-tocopherol solution (1 mg/mL) did not induce Yb.sup.3+ PL. Presumably, Yb.sup.3+ PL cannot be sensitized by these substances because they do not absorb visible light or they cannot modulate the absorption of NH.sub.2-TPDC linkers. Apart from producing interfering signals, interferants could also block the interactions between the target analyte and sensor. For instance, background molecules could adsorb to Yb—NH.sub.2-TPDC more favorably than gossypol and prevent gossypol from switching on Yb.sup.3+ luminescence. To assess the gossypol detection performance of Yb—NH.sub.2-TPDC in the presence of background substances, Yb.sup.3+ PL intensity at 976 nm in response to gossypol (100 mg/mL) without interferents was compared to PL intensity in the presence of cottonseed oil (100 mg/mL), palmitic acid (1 mg/mL), linoleic acid (1 mg/mL), and α-tocopherol (1 mg/mL), respectively. Although the concentrations of all tested interferents were at least 10 times higher than gossypol, the PL intensities of Yb—NH.sub.2-TPDC were largely unaffected. Overall, the Yb.sup.3+ PL of Yb—NH.sub.2-TPDC is selectively turned on by gossypol.

[0077] To determine the operative mechanism, Yb—NO.sub.2-TPDC was synthesized using 2′-nitro-1,1′:4′,1″-terphenyl-4,4″-dicarboxylic acid (H2-NO.sub.2-TPDC). Yb—NO.sub.2-TPDC and Yb—NH.sub.2-TPDC are isoreticular, as confirmed by PXRD. Lacking —NH.sub.2 groups, Yb—NO.sub.2-TPDC cannot react with gossypol to form a Schiff base. In the absence of gossypol, the NO.sub.2-TPDC linker does not sensitize Yb.sup.3+ PL at any excitation wavelengths. Incubating Yb—NO.sub.2-TPDC with gossypol solution, however, led to strong Yb.sup.3+ PL with excitation wavelengths spanning from 350 nm to 600 nm. Significantly, these experiments indicate, that gossypol is an effective sensitizer for Yb.sup.3+ PL. Further, no sign of Schiff base formation was observed after reacting Yb—NH.sub.2-TPDC with gossypol using the previously described method. In conclusion, the “turn-on” response of Yb.sup.3+ PL at 485 nm excitation is mainly due to the “antenna” effect of gossypol. As “antennae”, gossypol can sensitize Yb.sup.3+ PL of both Yb—NH.sub.2-TPDC and Yb—NO.sub.2-TPDC at excitation wavelengths greater than 525 nm, while gossypol in solution does not exhibit absorption above 480 nm. The large discrepancy between the gossypol excitation range in the MOF and its absorption band in solution is reminiscent of the above-mentioned observation with NH.sub.2-TPDC linker, and may also be attributed to confinement effects.

[0078] With strong evidence supporting that gossypol is an effective sensitizer for Yb.sup.3+ PL, other Ln materials for gossypol detection were evaluated. Since gossypol can form complexes with Ln3+ ions in solution, tests were conducted to determine whether simple and commercially available Ln.sup.3+ salts can be used as “turn-on” sensors for gossypol. Indeed, YbCl.sub.3.6H.sub.2O solution exhibited intense Yb.sup.3+ PL upon addition of gossypol. The excitation-emission map of an YbCl.sub.3.6H.sub.2O solution after 5 min incubation with gossypol showed that Yb.sup.3+ PL can be observed upon excitation from 330 nm to 480 nm. Compared to Yb—NH.sub.2-TPDC, the response time of YbCl.sub.3.6H.sub.2O is significantly faster, likely because gossypol molecules can readily access and coordinate Yb.sup.3+ ions in solution without overcoming the diffusion barriers posed by MOF pores. To determine the detection range of YbCl.sub.3.6H.sub.2O, emission spectra were collected 5 minutes after 1 mL of gossypol/acetone solution (0 μg/mL, 0.5 mg/mL, 1 μg/mL, 3 μg/mL, 5 μg/mL, 7μg/mL, 10 μg/mL, 25 μg/mL, 50 μg/mL) was added to 2 mL of YbCl.sub.3.6H.sub.2O/DMF solution (1 mg/mL). No emission was observed for the sample with acetone blank, while Yb.sup.3+ emission was observed for all samples containing gossypol. The limit of detection was determined to be 0.5 μg/mL (0.64 ppm) with a S/N of 10. The PL intensity at 976 nm followed a linear dependence with the concentration of gossypol solution between 0.5 μg/mL and 10 μg/mL and approached saturation at higher concentrations. In addition, it was discovered that the Nd.sup.3+ PL of NdCl.sub.3.6H.sub.2O at 1056 nm can also be used for gossypol detection in a similar fashion. Yb—NH.sub.2-TPDC and YbCl.sub.3.6H.sub.2O are complimentary and allow for detection and quantification of gossypol at different concentration ranges: from 0.5 μg/mL to 10 μg/mL using YbCl.sub.3.6H.sub.2O, and from 25 to 100 μg/mL using Yb—NH.sub.2-TPDC. In addition, Yb—NH.sub.2-TPDC can be advantageous for integration into solid state devices, whereas YbCl.sub.3.6H.sub.2Oprovides a simple way to rapidly and sensitively detect gossypol in solution.

[0079] In summary, it was discovered that gossypol, a toxic molecule that concerns the cotton industry, can effectively sensitize Yb.sup.3+ and Nd.sup.3+ NIR PL. As a result, there was demonstrated examples of luminescence “turn-on” detection of gossypol using Ln MOFs and Ln salts and achieved highly selective, fast-responding, and sensitive sensing of gossypol in acetone solution with a concentration of 0.5-100 μg/mL. This general sensing approach is applicable to the detection of a wide variety of aromatic molecules, including pharmaceuticals, pesticides, and other contaminants that may be present in water and food.

Example 2

[0080] The “turn-on” sensing of OH-Py carcinogenic PAHs biomarkers by amino and diamino functionalized MOFs was evaluated. The 2-amino-1,4-benzenedicarboxylic acid (H.sub.2-NH.sub.2-BDC) and 2,5-diamino-1,4-benzenedicarboxylic acid (H.sub.2-2NH.sub.2-BDC) were reacted with TbCl.sub.3.6H.sub.2O in a mixture of dimethylformamide (DMF), water and nitric acid solution at 120° C. and yielded colorless and brown-black cubic crystals denoted as {[(Me.sub.2NH.sub.2).sub.2.[Tb.sub.6(C.sub.8H.sub.5NO.sub.2).sub.6.6H.sub.2O].12DMF}.sub.n(Tb—NH2-BDC) and {[(Me.sub.2NH.sub.2).sub.2.[Tb.sub.6(C.sub.8H.sub.6NO.sub.2).sub.6.6H.sub.2O].10DMF}.sub.nTb-2NH.sub.2-BDC, respectively. Both MOFs were characterized by numerous analytical techniques.

[0081] The emission spectra of activated Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC upon incremental addition of OH-Py resulted in quenching when excited in the range of 280-370 nm. This result depicted the attenuation of incident light due to the photoinduced electron transfer (PET) or Forster resonance energy transfer (FRET) process in the presence of OH-Py. These experiments indicated that after excitation beyond 370 and up to 410 nm the turn-on emission was observed in the presence of OH-Py. The turn-on sensing ability of activated Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC towards OH-Py upon excitation at 375 nm was then evaluated. The typical fluorometric titration of OH-Py (1 mM stock solution; 2.5-300 μL, each) showed turn-on signature at 407 and 408 nm. The detection limit (LoD, 36/m) of activated Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC were found to be 19 and 59 parts per billion (ppb) for OH-Py, respectively. The fast response of OH-Py in presence of both MOFs suggested the diffusion and mass transfer of both analyte in the pore channels.

[0082] For real-time applications, selective fluorescence turn-on titration experiment of activated Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC towards other urine components such as uric acid, hippuric acid (Hipp), creatine, creatinine, urea, glucose, NH.sub.4Cl, NaCl and KCl under the same condition (λexc: 375 nm, 1 mM stock solution; 10-300 μL each, measured after every one minute), were performed. This fluorescent titration experiment depicted that both MOFs exhibited highly selective turn-on response towards OH-Py, whereas negligible to moderate response observed for other urine components under the same conditions. This was because the rest of the urine analytes cannot absorb visible light or modulate the absorption of Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC. Therefore, except OH-Py other interfering urine components cannot excite under 375 nm and missing the spectral overlap. Both the MOFs exhibited good recyclability after turn-on detection. These results demonstrate that both Tb—NH.sub.2-BDC and Tb-2NH.sub.2-BDC are an efficient turn-on sensor for OH-Py and for real-time applications.