rotational isomer
1rotamer — A rotational isomer conformationally different by rotation at a single bond …
2isomerism — /uy som euh riz euhm/, n. 1. Chem. the relation of two or more compounds, radicals, or ions that are composed of the same kinds and numbers of atoms but differ from each other in structural arrangement (structural isomerism), as CH3OCH3 and… …
3Glucose — This article is about the naturally occurring D form of glucose. For the L form, see L Glucose. D glucose …
4Synthetic molecular motors — are molecular machines capable of rotation under energy input. Although the term molecular motor has traditionally referred to a naturally occurring protein that induces motion, some groups also use the term when referring to non biological, non… …
5Mössbauer spectroscopy — A Mössbauer absorption spectrum of 57Fe Mössbauer spectroscopy is a spectroscopic technique based on the Mössbauer effect. This effect, discovered by Rudolf Mössbauer in 1957, consists in the recoil free, resonant absorption and emission of gamma …
6Physical Sciences — ▪ 2009 Introduction Scientists discovered a new family of superconducting materials and obtained unique images of individual hydrogen atoms and of a multiple exoplanet system. Europe completed the Large Hadron Collider, and China and India took… …
7Chirality (chemistry) — L form redirects here. For the bacterial strains, see L form bacteria. Two enantiomers of a generic amino acid …
8Conformational isomerism — Conformers of butane, shown in Newman projection. The two gauche as well as the anti form are staggered conformations In chemistry, conformational isomerism is a form of stereoisomerism in which the isomers can be interconverted exclusively by… …
9radioactivity — /ray dee oh ak tiv i tee/, n. Physics, Chem. the phenomenon, exhibited by and being a property of certain elements, of spontaneously emitting radiation resulting from changes in the nuclei of atoms of the element. Also called activity. [1895… …
10Asymmetric induction — (also enantioinduction) in stereochemistry describes the preferential formation in a chemical reaction of one enantiomer or diastereoisomer over the other as a result of the influence of a chiral feature present in the substrate, reagent,… …
