## Abstract The vapor‐phase optical rotation (or circular birefringence) of (__S__)‐1,2‐epoxybutane, (__S__)‐epichlorohydrin, and (__S__)‐epifluorohydrin has been measured at the nonresonant excitation wavelengths of 355 nm and 633 nm by means of Cavity Ring‐Down Polarimetry (CRDP). Complementary s
Specific anion effects on the optical rotation of glucoseand serine
✍ Scribed by Pierandrea Lo Nostro; Barry W. Ninham; Silvia Milani; Laura Fratoni; Piero Baglioni
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2006
- Tongue
- English
- Weight
- 534 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
Optical activity is directly related to molecular conformation through the anisotropic polarizabilities of molecules and the refractive index of materials. L‐amino acids and D‐sugars are characteristic essential bioactive molecules. Since molecular recognition and enzyme activity are related to the conformation of substrates, the relevance of optical activity to biological processes is evident. Specific ion, or Hofmeister, effects that occur with electrolytes at moderately high concentrations modify the behavior of interfaces, molecular forces between membranes, of bulk solutions, of enzymes, and even of DNA. Such effects are universal. Here we report a study on the change in optical rotation induced by some sodium salts for the enantiomers of serine and glucose in water solution. The optical rotation is shown to depend on the kind of anion and on the salt concentration. To obtain further insights into the mechanism behind the phenomenon, Fourier transform infrared (FTIR) spectral studies of serine and glucose solutions in electrolytes were also carried out. The results suggest that it is the differences in interactions of anions at specific chemical sites of the solutes that are responsible for the effects. These forces depend strongly on anion polarizability in water. Such specific ion preferential interactions can affect conformation and internal field, and result in significant changes in optical rotation. © 2005 Wiley Periodicals, Inc. Biopoly 81: 136–148, 2006
This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at [email protected]
📜 SIMILAR VOLUMES
It is shown ikat linear electro-optical rotation is always zero as ion& as it is considered ritr; a. conventional two-photon effect. It follows aI60 tkat quadratic electrr-opttcat rotation is zero if the field is taken along the beam OF light.
## Abstract A computational investigation of the optical rotatory power of __cis__ and __trans__ 2‐methyl‐5‐oxo‐tetrahydro‐3‐furancarboxylic acids and the corresponding methyl and ethyl esters is presented. Solvent effects on both the conformational space and the rotatory power are analyzed by comp