Dynamic and Static Behavior of E-E' Bonds in Neutral and Charged Forms of HEE'H, MeEE'Me, andCyclo-1,2-EE'(CH2)3(E, E' = O, S, Se, and Te) Elucidated by AIM Dual Functional Analysis-Reference-Cited by-同舟云学术

Dynamic and Static Behavior of E-E' Bonds in Neutral and Charged Forms of HEE'H, MeEE'Me, andCyclo-1,2-EE'(CH2)3(E, E' = O, S, Se, and Te) Elucidated by AIM Dual Functional Analysis

Published:2014-06-24 Issue:5 Volume:25 Page:449-472
ISSN:1042-7163
Container-title:Heteroatom Chemistry
language:en
Short-container-title:Heteroatom Chem.

Author:

Hayashi Satoko¹,Matsuiwa Kohei¹,Miza Hiroaki¹,Nakanishi Waro¹

Affiliation:

1. Department of Material Science and Chemistry; Faculty of Systems Engineering, Wakayama University; 930 Sakaedani Wakayama 640-8510 Japan

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/hc.21194/fullpdf

Reference73 articles.

1. Preliminary discussion for the neutral form of HEE'H and MeEE'Me (E, E' = S, Se, and Te) Hayashi , S. Miza , H. Nakanishi , W. Invited Paper on the First Electronic Symposium on Selenium Chemistry eSeS-1, dedicated to Professor M. Tiecco on his retirement http://eses1.chimfarm.unipg.it 2011 The θ p value of 198.3° for HS-*-SeH in Table 2 of the reference should be read 189.3°

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3. Transannular E···E′ Interactions in Neutral, Radical Cationic, and Dicationic Forms of cyclo-[E(CH2CH2CH2)2E′] (E, E′ = S, Se, Te, and O) with Structural Feature: Dynamic and Static Behavior of E···E′ Elucidated by QTAIM Dual Functional Analysis;The Journal of Organic Chemistry;2015-12-04

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