A system, method and computer program product for detecting indicators for structural changes of NMR active test molecules in a test sample, or indicators for structural changes of the environment of said test molecules in relation to a reference molecule. Initial local similarity values are obtained, using a similarity function and representing a local similarity between a reference spectrum and a test spectrum within corresponding similarity regions (SRR, SRT). The initial local similarity values represent a similarity map (SM1) in which contours of a first shape type are indicators (I1) for structural changes of the test molecule, and in which contours of a second shape type are indicators (I2) for structural changes of the environment of said test molecule in relation to the reference molecule.

An exemplary integrated nuclear quadrupole resonance-based detection system comprises a front-end device having a hand-held form factor, wherein the front-end device is configured to scan a sample in or near a sample coil using inbuild electronics and acquire a nuclear quadrupole resonance measurement. The system further includes a swappable sample coil that is attached to an opening at a face of the front-end device and is tuned to a resonant frequency of the sample; and a swappable impedance matching network that is attached to the opening at the face of the front-end device and is configured to tune the resonant frequency of the sample coil. The inbuild electronics comprises a wireless transfer module that is configured to communicate the acquired nuclear quadrupole resonance measurement with a back-end device of the integrated nuclear quadrupole resonance-based detection system. Other systems and methods are also provided.

Provided is a method of analyzing a copolycarbonate. More particularly, provided is a method of analyzing a copolycarbonate, in which a polysiloxane structure is introduced into the main chain of a polycarbonate, the method capable of more accurately analyzing a weight average molecular weight, a number average molecular weight, and a molecular weight distribution of a polysiloxane-containing aromatic diol compound which is used as a starting material.

This disclosure relates to the identification of interactions between ligands and in-membrane proteins using nuclear magnetic resonance spectroscopy. Also provided are methods for high-throughput identification of in-membrane ligand-membrane protein interactions.

A film for a light emitting device which is useful for producing a light emitting device having excellent luminance life is described. The film contains a cross-linked body of a crosslinkable material having a crosslinking group in an amount of 0.015 mmol/g to 0.05 mmol/g. A light emitting device containing the film is also described. A method for analyzing a crosslinking group in a film for a light emitting device involves: (1) a step of swelling the above-described film for a light emitting device with a solvent, and (2) a step of measuring a crosslinking group of the swollen film for a light emitting device using nuclear magnetic resonance spectroscopy.

Method of obtaining a fingerprint from Cannabis samples comprising the following steps: determination of the genetic profile by analysis of at least one STR marker, obtaining the chemical profile by NMR, and differentiation of cannabis varieties from each other by comparing the results obtained in steps (a) and (b) on each sample with each other and/or with previously obtained fingerprint databases.

Molecular rotational resonance (MRR) spectroscopy is a structurally-specific, high-resolution spectroscopy technique that can provide accurate reaction process data with finer time resolution than existing techniques. It is the only analytical technique that can make online chiral composition measurements. This makes it especially useful for online reaction monitoring, which is done today by manually pulling off samples and measuring samples offline and takes 3-4 hours per measurement. Conversely, an MRR spectrometer can resolve isomers in about 10 minutes when fed with a low-volatility sampling interface that connects directly to the reaction line. The sampling interface measures a precise sample of the reaction solution, boils off the solvent to concentrate the analyte, volatilizes the analyte, and injects the volatilized analyte into the MRR spectrometer's measurement chamber for an MRR measurement. The sample concentration and volatilization happen quickly and without any extra sample preparation.

A composition comprising an ethylene/alpha-olefin/non-conjugated polyene, and wherein the ethylene/alpha-olefin/non-conjugated polyene comprises the following property: a “13C NMR % iCB Peak Area,” which is the {[(13C NMR peak area from 34.4 ppm to 34.6 ppm) divided by (the 13C NMR sum integral area from 160.0 to 100.0 and from 60.0 ppm to 0.00 ppm)]×100}, that is >0.010%, as determined by 13C NMR.

The present application relates to a composition comprising the following components: A) at least one ethylene/alpha-olefin interpolymer; B) a peroxide; C) at least one filler selected from one or more carbon black samples, MgO, or a combination thereof; and optionally, at least one filler selected from silica, ZnO, CaCO.sub.3, A1 (OH).sub.3, Mg (OH).sub.2, or a combination thereof; D) a calculated P content from 0.010 wt % to 0.300 wt %, based on the weight of the composition, and wherein the calculated P content is the calculated content the phosphorus element present in one or more phosphate compounds selected from Structure 1 below: O═P (OR1) (OR2) (OR3) (Structure 1), wherein R1, R2 and R3 are each, independently, selected from i) a non-aromatic hydrocarbon or ii) a non-aromatic hydrocarbon comprising at least one heteroatom, excluding P.

The present disclosure relates to a heterochiral peptide complex, a self-assembled intermediate thereof, an alignment medium composition used for nuclear magnetic resonance spectroscopy residual dipolar coupling (NMR-RDC) measurement, which includes the same, and a method for NMR measurement for a biomolecule. Since the heterochiral peptide complex contains a β-sheet peptide and has superior structural stability against environmental factors such as heat, acidity and ionic strength, it is applicable as an alignment medium for measuring RDC for various biomolecules.