Literature DB >> 26262562

London dispersion in molecular chemistry--reconsidering steric effects.

J Philipp Wagner1, Peter R Schreiner2.   

Abstract

London dispersion, which constitutes the attractive part of the famous van der Waals potential, has long been underappreciated in molecular chemistry as an important element of structural stability, and thus affects chemical reactivity and catalysis. This negligence is due to the common notion that dispersion is weak, which is only true for one pair of interacting atoms. For increasingly larger structures, the overall dispersion contribution grows rapidly and can amount to tens of kcal mol(-1) . This Review collects and emphasizes the importance of inter- and intramolecular dispersion for molecules consisting mostly of first row atoms. The synergy of experiment and theory has now reached a stage where dispersion effects can be examined in fine detail. This forces us to reconsider our perception of steric hindrance and stereoelectronic effects. The quantitation of dispersion energy donors will improve our ability to design sophisticated molecular structures and much better catalysts.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords:  density functional theory; noncovalent interactions; van der Waals forces; weak interactions

Year:  2015        PMID: 26262562     DOI: 10.1002/anie.201503476

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  91 in total

1.  Dynamic Kinetic Resolution of Aldehydes by Hydroacylation.

Authors:  Zhiwei Chen; Yusuke Aota; Hillary M H Nguyen; Vy M Dong
Journal:  Angew Chem Int Ed Engl       Date:  2019-02-27       Impact factor: 15.336

2.  On the ability of pnicogen atoms to engage in both σ and π-hole complexes. Heterodimers of ZF2C6H5 (Z = P, As, Sb, Bi) and NH3.

Authors:  Wiktor Zierkiewicz; Mariusz Michalczyk; Rafał Wysokiński; Steve Scheiner
Journal:  J Mol Model       Date:  2019-05-08       Impact factor: 1.810

3.  Formation of active species from ruthenium alkylidene catalysts-an insight from computational perspective.

Authors:  Paweł Śliwa; Mariusz P Mitoraj; Filip Sagan; Jarosław Handzlik
Journal:  J Mol Model       Date:  2019-11-07       Impact factor: 1.810

4.  Delayed catalyst function enables direct enantioselective conversion of nitriles to NH2-amines.

Authors:  Shaochen Zhang; Juan Del Pozo; Filippo Romiti; Yucheng Mu; Sebastian Torker; Amir H Hoveyda
Journal:  Science       Date:  2019-04-05       Impact factor: 47.728

5.  Enantioselective Synthesis of N,S-Acetals by an Oxidative Pummerer-Type Transformation using Phase-Transfer Catalysis.

Authors:  Souvagya Biswas; Koji Kubota; Manuel Orlandi; Mathias Turberg; Dillon H Miles; Matthew S Sigman; F Dean Toste
Journal:  Angew Chem Int Ed Engl       Date:  2017-12-12       Impact factor: 15.336

6.  Pursuit of Noncovalent Interactions for Strategic Site-Selective Catalysis.

Authors:  F Dean Toste; Matthew S Sigman; Scott J Miller
Journal:  Acc Chem Res       Date:  2017-03-21       Impact factor: 22.384

7.  Application of Q2MM to predictions in stereoselective synthesis.

Authors:  Anthony R Rosales; Taylor R Quinn; Jessica Wahlers; Anna Tomberg; Xin Zhang; Paul Helquist; Olaf Wiest; Per-Ola Norrby
Journal:  Chem Commun (Camb)       Date:  2018-07-24       Impact factor: 6.222

8.  Structure-Activity Studies of Semiochemicals from the Spider Orchid Caladenia plicata for Sexual Deception.

Authors:  Bjorn Bohman; Amir Karton; Gavin R Flematti; Adrian Scaffidi; Rod Peakall
Journal:  J Chem Ecol       Date:  2018-03-17       Impact factor: 2.626

9.  Questions in natural products synthesis research that can (and cannot) be answered using computational chemistry.

Authors:  Dean J Tantillo
Journal:  Chem Soc Rev       Date:  2018-10-29       Impact factor: 54.564

10.  Catalytic diastereo- and enantioselective additions of versatile allyl groups to N-H ketimines.

Authors:  Hwanjong Jang; Filippo Romiti; Sebastian Torker; Amir H Hoveyda
Journal:  Nat Chem       Date:  2017-07-17       Impact factor: 24.427

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.