Literature DB >> 29999196

Thermoresponsive Alignment Media in NMR Spectroscopy: Helix Reversal of a Copolyaspartate at Ambient Temperatures.

Mira Schwab1, Volker Schmidts1, Christina M Thiele1.   

Abstract

Poly(aspartic acid esters) are known to form either right-or left-handed α-helices depending on the ester group in the side chain, on solvent and/or on temperature. Polyphenethyl-l-aspartates (PPLA) exhibit a helix reversal from the right- to the left-handed form with increasing temperature. We have recently reported the application of polyphenethylaspartates as helically chiral alignment media. The thermoresponsivity observed for these polymers offers the possibility to measure different orientations of analytes before and after helix reversal of the alignment medium at 373 K. Herein we present a synthesized copolymer of phenethyl- and benzylaspartate as a new alignment medium undergoing this helix reversal at 303-313 K. Thus, the measurement of residual dipolar couplings (RDC) before and after the helix reversal is allowed for at ambient temperatures. A complete sign change of all 1 H-13 C RDCs was observed, which is close to the highest possible difference in NMR spectra.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  NMR spectroscopy; alignment media; helix reversal; liquid crystals; polyaspartates; residual dipolar couplings

Mesh:

Substances:

Year:  2018        PMID: 29999196     DOI: 10.1002/chem.201803540

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Synergism of anisotropic and computational NMR methods reveals the likely configuration of phormidolide A.

Authors:  Ikenna E Ndukwe; Xiao Wang; Nelson Y S Lam; Kristaps Ermanis; Kelsey L Alexander; Matthew J Bertin; Gary E Martin; Garrett Muir; Ian Paterson; Robert Britton; Jonathan M Goodman; Eric J N Helfrich; Jörn Piel; William H Gerwick; R Thomas Williamson
Journal:  Chem Commun (Camb)       Date:  2020-07-09       Impact factor: 6.222

2.  The Advanced Floating Chirality Distance Geometry Approach-How Anisotropic NMR Parameters Can Support the Determination of the Relative Configuration of Natural Products.

Authors:  Matthias Köck; Michael Reggelin; Stefan Immel
Journal:  Mar Drugs       Date:  2020-06-24       Impact factor: 5.118

3.  NMR-Based Configurational Assignments of Natural Products: Gibbs Sampling and Bayesian Inference Using Floating Chirality Distance Geometry Calculations.

Authors:  Stefan Immel; Matthias Köck; Michael Reggelin
Journal:  Mar Drugs       Date:  2021-12-22       Impact factor: 5.118

  3 in total

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