JOURNAL ARTICLE

η6-Indene- and η5-indole-(pentamethylcyclopentadienyl)-rhodium(III) and -iridium(III) hexafluorophosphates and their reversible deprotonation and rearrangement reactions to η5-indenyl- and η5-indolyl-complexes

Colin WhiteStephen J. ThompsonPeter M. Maitlis

Year: 1976 Journal:   Journal of the Chemical Society Chemical Communications Pages: 409-410   Publisher: Royal Society of Chemistry

Abstract

The preparations of [M(η5-C5Me5)(η6-indene)](PF6)2, (II), [M(η5-C5Me5)(η5-indenyl)](PF6),(III),[M(η5-C5Me5)(η5-indole)](PF6)2(M = Rh or Ir), and [Ir(η5-C5Me5)(η5-indolyl)]PF6 are reported; in the interconversion (III)+ H+⇌(II), for M = Ir protonation-deprotonation is fast and the rate-determining step is the movement of the metal from the 5- to the 6-membered ring and vice-versa.

Keywords:
Deprotonation Iridium Chemistry Indene Protonation Indole test Rhodium Ring (chemistry) Medicinal chemistry Stereochemistry Catalysis Organic chemistry Ion

Metrics

13
Cited By
3.18
FWCI (Field Weighted Citation Impact)
0
Refs
0.88
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Fluorine in Organic Chemistry
Life Sciences →  Pharmacology, Toxicology and Pharmaceutics →  Pharmaceutical Science
Catalytic C–H Functionalization Methods
Physical Sciences →  Chemistry →  Organic Chemistry
Catalytic Cross-Coupling Reactions
Physical Sciences →  Chemistry →  Organic Chemistry

Related Documents

© 2026 ScienceGate Book Chapters — All rights reserved.