Altering thermochromic transition temperature in transition metal ethylenediamine complexes by substitutional doping of anionic species

Abstract

Tunable thermochromic materials comprise a metal salt with a varying proportion of two different anions and an organic ligand. Partial substitution via doping during the initial synthesis with a macro-structurally similar (generating an isostructural material) yet chemically different anion creates a material with altered thermochromic properties. For example, in bromide-doped bis(N,N-diethylethylenediamine)nickel(II)) tetrafluoroborate; both the tetrafluoroborate (BF4-) and bromide (Br) derivatives are isostructural. Substitution of BF4- for Br causes a decrease in the materials' thermochromic transition temperature by approximately 10? C.

Claims

1. A tunable thermochromic material comprising: a first instance of an organic ligand complexed with a metal salt; and two different anions present in a first proportion; and a second instance of the organic ligand complexed with the metal salt and the two different anions, wherein the two different anions are present in a second proportion differing from the first proportion, wherein, as a consequence of the different proportions, the first instance has a different thermochromic transition temperature from that of the second instance, wherein the thermochromic transition is reversible with a change in temperature, and wherein the organic ligand is an N,N-disubstituted diamine.

2. The material of claim 1, wherein the anions are selected from the group consisting of BF.sub.4.sup.?, ClO.sub.4.sup.?, NO.sub.3.sup.?, Br.sup.?, and I.sup.?.

3. A tunable thermochromic material comprising: a first instance of N,N-diethylethylenediamine operating as a ligand and complexed with a metal salt; and two different anions present in a first proportion, wherein the anions are tetrafluoroborate (BF.sub.4.sup.?) and bromide (Br.sup.?); and a second instance of N,N-diethylethylenediamine operating as a ligand complexed with the metal salt and the two different anions, wherein the two different anions are present in a second proportion differing from the first proportion, wherein, as a consequence of the different proportions, the first instance has a different thermochromic transition temperature from that of the second instance, and wherein the thermochromic transition is reversible with a change in temperature.

4. The material of claim 3, wherein the metal salt comprises nickel.

5. A method of preparing a tunable thermochromic material, the method comprising: providing in a first solvent two different anions present in a first proportion and a metal salt; adding an organic ligand to the solvent, thereby causing a first thermochromic material to precipitate; providing in a second solvent the two different anions present in a second proportion and the metal salt; adding the organic ligand to the second solvent, thereby causing a second thermochromic material to precipitate, wherein the first and second thermochromic materials differ only in the proportions of the two different anions, wherein the ligand is an N,N-disubstituted diamine, and wherein, as a consequence of the different proportions, the first material has a different thermochromic transition temperature from that of the second material, and wherein the thermochromic transition is reversible with a change in temperature.

6. The method of claim 5, wherein the anions are selected from the group consisting of BF.sub.4.sup.?, ClO.sub.4.sup.?, NO.sub.3.sup.?, Br.sup.?, and I.sup.?.

7. The method of claim 5, wherein the ligand is N,N-diethylethylenediamine.

8. The method of claim 5, wherein: the anions are tetrafluoroborate (BF.sub.4.sup.?) and bromide (Br.sup.?); the metal salt comprises nickel; and the ligand is N,N-diethylethylenediamine.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 provides a synthetic scheme for the preparation of bromide-doped bis(N,N-diethylethylenediamine)nickel(II)) tetrafluoroborate having varying proportions of tetrafluoroborate (BF.sub.4.sup.?) and bromide (Br.sup.?).

(2) FIG. 2 shows the thermochromic transition temperature depression with increasing percentage of bromide substitution.

DETAILED DESCRIPTION

Definitions

(3) Before describing the present invention in detail, it is to be understood that the terminology used in the specification is for the purpose of describing particular embodiments, and is not necessarily intended to be limiting. Although many methods, structures and materials similar, modified, or equivalent to those described herein can be used in the practice of the present invention without undue experimentation, the preferred methods, structures and materials are described herein. In describing and claiming the present invention, the following terminology will be used in accordance with the definitions set out below.

(4) As used herein, the singular forms a, an, and the do not preclude plural referents, unless the content clearly dictates otherwise.

(5) As used herein, the term and/or includes any and all combinations of one or more of the associated listed items.

(6) As used herein, the term about when used in conjunction with a stated numerical value or range denotes somewhat more or somewhat less than the stated value or range, to within a range of ?10% of that stated.

(7) Overview

(8) The synthesis of doped thermochromic metal complexes with various divalent metal centers and monovalent anionic lattice moieties is achieved by rapid precipitation from anhydrous alcohol (ROH where R?CH.sub.3, C.sub.2H.sub.5, etc.) of dissolved metal ions and monovalent anions with the dropwise addition of N,N-dialkyl or -arylethylenediamine Generally, two anhydrous alcohol solutions are formed with two different metal salts, with chemical formula MX.sub.2 (where M is Ni.sup.2+ or Cu.sup.2+ and X=a monovalent anionic species, e.g. BF.sub.4.sup.?, ClO.sub.4.sup.?, NO.sub.3.sup.? or Br.sup.?),such as Ni(BF.sub.4).sub.2, with the same divalent metal specie (e.g. Ni(BF.sub.4).sub.2 and NiBr.sub.2). The concentrations of these solutions are added stoichiometrically such that the desired doping percentage of the monovalent anionic species are established. These two solutions are then combined and two equivalents (compared to the Ni.sup.2+ concentrations) of N,N-disubstituted diamine is added dropwise, resulting in almost immediate precipitation of the desired product, which exhibits a reversible thermochromic transition.

Example

(9) Nickel diethylethylenediamine tetrafluoroborate/bromide, Ni[C.sub.6H.sub.16N.sub.2].sub.2.Math.(BF.sub.4).sub.1.5/(Br).sub.0.5 was prepared as follows. To a 1 dram glass shell vial, one added 1 mL of 0.5 M Ni(BF.sub.4).sub.2 in anhydrous ethanol, 0.17 mL of 0.5 M NiBr.sub.2 in anhydrous ethanol, and 0.830 mL of anhydrous ethanol to form a clear green solution. To that solution, one added 0.094 mL of N,N-diethylethylenediamine. The yellow-orange solid precipitated almost immediately, was filtered and washed with anhydrous ethanol, and dried at 65? C. overnight in an oven to produce stoichiometric yield.

(10) Additional details are provided in Inorg. Chem. 2022, 61, 23, 8834-8842 and accompanying Supporting Information, all of which is incorporated herein by reference for the purposes of disclosing techniques for preparing and analyzing thermochromic complexes.

Further Embodiments

(11) Other monovalent anions may be utilized as the matrix lattice moieties, those which are the majority phase in the material, or the dopant lattice moieties. These anion species may consist of, but are not limited to, compounds containing anions such as BF.sub.4.sup.?, ClO.sub.4.sup.?, NO.sub.3.sup.?, Br.sup.?, and I.sup.?. The synthetic process remains essentially the same for all combinations of anions, metal centers, and N,N-disubstituted diamines.

(12) These materials could be used to generate complex unique thermochromic signatures that are easy to read and difficult to mimic, making this technology potentially relevant for document security and anti-counterfeiting measures as well as for other chemical taggant applications.

Advantages

(13) This methodology represents a new way of modifying a family of thermochromic materials through doping various monovalent anionic lattice moieties so as to produce a targeted spectroscopic and colorimetric response. The partial substitution doping is a synthetic alteration to influence the thermochromic transition to lower temperatures in a way that does not fundamentally change the structure or stability of the material itself. Doping in the macro-structurally similar, yet chemically different monovalent anion subtly influences the hydrogen bonding network between the metal complex and the charge-balancing lattice anion, altering the mechanism of thermochromism. Varying the doping percentage creates a variable and tunable spectroscopic signature, wherein the transition temperature decreases with increasing doping percentage.

(14) Current inorganic or hybrid (contains a metal or a metal and organic component) thermochromic materials have several limitations for technological applications relating to their environmental and public health safety and thermochromic transition temperature. Many inorganic thermochromic materials contain mercury, lead, chromium, etc. in high concentrations (Cu.sub.2[HgI.sub.4]) or as dopants in less toxic matrices (chromium in aluminum oxide). Further, these materials are often constrained to specific transition temperatures with limited potential for manipulation or suffer from a lack of transition temperature specificity, meaning the transition occurs over a wide temperature regime (tens or hundreds or degrees). The materials described herein represent a class of compounds with temperature specific and optically obvious dramatic changes in color which can be manipulated during synthesis via doping to exhibit thermochromism at variable temperatures while retaining the material properties of the un-doped compound. Also, for example, thermal stability of bis(N,N-diethylethylenediamine)nickel(II) tetrafluoroborate is retained up to 260? C. Taking into consideration all materials within this class of compounds, and the observed 10? C. shift in temperature due to doping a broad range of transition temperatures from 10? C. to 200? C. are feasible.

CONCLUDING REMARKS

(15) All documents mentioned herein are hereby incorporated by reference for the purpose of disclosing and describing the particular materials and methodologies for which the document was cited.

(16) Although the present invention has been described in connection with preferred embodiments thereof, it will be appreciated by those skilled in the art that additions, deletions, modifications, and substitutions not specifically described may be made without departing from the spirit and scope of the invention. Terminology used herein should not be construed as being means-plus-function language unless the term means is expressly used in association therewith.

REFERENCES

(17) Pfeiffer, P; Glaser, H. J. Prakt. Chem. 1938, 151, 134. Thermochromism in Copper(II) Complexes. Structures of the Red and Blue-Violet Forms of Bis(N,N-diethylethylenediamine)copper(II) Perhlorate and the Nonthermochromic Violet Bis(N-ethylethylenediamine)copper(II) Perhlorate. Grenthe, I.; Paoletti, P.; Sandstrom M.; Glikberg S. Inorg. Chem. 1979 18. 10. 2687-2692.