Literature DB >> 17924421

Why is it important to simultaneously use more than one chiroptical spectroscopic method for determining the structures of chiral molecules?

Prasad L Polavarapu1.   

Abstract

In recent years, four different chiroptical spectroscopic methods, namely vibrational circular dichroism, vibrational Raman optical activity, electronic circular dichroism, and optical rotatory dispersion, have become popular for establishing the absolute configuration and predominant conformations of chiral molecules in solution state. Many individual laboratories normally utilize only one of these methods to derive the molecular structural information. Although that approach may be satisfactory for most of the molecules studied, it is to be noted that in some instances a single method can give ambiguous conclusions or may not give complete structural information. This article summarizes the situations where simultaneous use of more than one chiroptical spectroscopic method is required to obtain molecular structural information and recommends the routine application of more than one chiroptical spectroscopic method for any given molecule. Copyright 2007 Wiley-Liss, Inc.

Year:  2008        PMID: 17924421     DOI: 10.1002/chir.20475

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  16 in total

1.  Chiroptical spectra of a series of tetrakis((+)-3-heptafluorobutylyrylcamphorato)lanthanide(III) with an encapsulated alkali metal ion: circularly polarized luminescence and absolute chiral structures for the Eu(III) and Sm(III) complexes.

Authors:  Jamie L Lunkley; Dai Shirotani; Kazuaki Yamanari; Sumio Kaizaki; Gilles Muller
Journal:  Inorg Chem       Date:  2011-11-10       Impact factor: 5.165

2.  Optical signatures of molecular dissymmetry: combining theory with experiments to address stereochemical puzzles.

Authors:  Parag Mukhopadhyay; Peter Wipf; David N Beratan
Journal:  Acc Chem Res       Date:  2009-06-16       Impact factor: 22.384

3.  Reassignment of the absolute configuration of plakinidone from the sponge consortium Plakortis halichondrioides-Xestospongia deweerdtae using a combination of synthesis and a chiroptical approach.

Authors:  Carlos Jiménez-Romero; Joanna E Rode; Abimael D Rodríguez
Journal:  Tetrahedron Asymmetry       Date:  2016-04-07

4.  A single chiroptical spectroscopic method may not be able to establish the absolute configurations of diastereomers: dimethylesters of hibiscus and garcinia acids.

Authors:  Prasad L Polavarapu; Emily A Donahue; Ganesh Shanmugam; Giovanni Scalmani; Edward K Hawkins; Carmelo Rizzo; Ibrahim Ibnusaud; Grace Thomas; Deenamma Habel; Dellamol Sebastian
Journal:  J Phys Chem A       Date:  2011-05-13       Impact factor: 2.781

5.  Importance of solvation in understanding the chiroptical spectra of natural products in solution phase: garcinia acid dimethyl ester.

Authors:  Prasad L Polavarapu; Giovanni Scalmani; Edward K Hawkins; Carmelo Rizzo; Neha Jeirath; Ibrahim Ibnusaud; Deenamma Habel; Divya Sadasivan Nair; Simimole Haleema
Journal:  J Nat Prod       Date:  2010-11-29       Impact factor: 4.050

Review 6.  Absolute configurations of DNA lesions determined by comparisons of experimental ECD and ORD spectra with DFT calculations.

Authors:  Shuang Ding; Alexander Kolbanovskiy; Alexander Durandin; Conor Crean; Vladimir Shafirovich; Suse Broyde; Nicholas E Geacintov
Journal:  Chirality       Date:  2009       Impact factor: 2.437

7.  Absolute configuration of actinophyllic acid as determined through chiroptical data.

Authors:  Tohru Taniguchi; Connor L Martin; Kenji Monde; Koji Nakanishi; Nina Berova; Larry E Overman
Journal:  J Nat Prod       Date:  2009-03-27       Impact factor: 4.050

8.  Absolute configurations of spiroiminodihydantoin and allantoin stereoisomers: comparison of computed and measured electronic circular dichroism spectra.

Authors:  Shuang Ding; Lei Jia; Alexander Durandin; Conor Crean; Alexander Kolbanovskiy; Vladimir Shafirovich; Suse Broyde; Nicholas E Geacintov
Journal:  Chem Res Toxicol       Date:  2009-06       Impact factor: 3.739

9.  Luminescent and Chiroptical Properties of 1 : 1 Eu (III) : Tetracycline Species Probed by Circularly Polarized Luminescence.

Authors:  Kirandeep K Deol; Gilles Muller
Journal:  Chempluschem       Date:  2019-11-22       Impact factor: 2.863

Review 10.  VCD studies on chiral characters of metal complex oligomers.

Authors:  Hisako Sato; Akihiko Yamagishi
Journal:  Int J Mol Sci       Date:  2013-01-07       Impact factor: 5.923

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.