z-logo
Premium
trans Influences on Hypervalent Bonding of Aryl λ 3 ‐Iodanes: Their Stabilities and Isodesmic Reactions of Benziodoxolones and Benziodazolones
Author(s) -
Ochiai Masahito,
Sueda Takuya,
Miyamoto Kazunori,
Kiprof Paul,
Zhdankin Viktor V.
Publication year - 2006
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.200603055
Subject(s) - hypervalent molecule , isodesmic reaction , zigzag , monomer , chemistry , aryl , medicinal chemistry , stereochemistry , polymer , crystallography , molecule , alkyl , organic chemistry , mathematics , geometry , reagent
Large and small or twice moderate : Both combinations of trans influences of the substituents favor the formation of highly stable aryl λ 3 ‐iodanes ArILL′ (examples: PhI(OH)OTs and PhI(OAc) 2 ). trans influences also seem to explain why iodosylbenzene adopts an oxo‐bridged zigzag polymer structure in contrast to PhI(OH) 2 , which is monomeric.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom