Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

C-H activation induced by water. Monocyclometalated to dicyclometalated: C boolean AND N boolean AND C tridentate platinum complexes

Tools
- Tools
+ Tools

UNSPECIFIED (2000) C-H activation induced by water. Monocyclometalated to dicyclometalated: C boolean AND N boolean AND C tridentate platinum complexes. ORGANOMETALLICS, 19 (7). pp. 1355-1364. ISSN 0276-7333

Full text not available from this repository.

Abstract

Metalation of 2,6-diphenylpyridine (1) by potassium tetrachloroplatinate in acetic acid gives a monocyclometalated chloride-bridged dimer 4. This dimer is split with CO to give a kinetic product st with the incoming CO trans to the orthometalated carbon. The kinetic product of cleavage is shown to be 16 kJ mol(-1) higher in energy than the thermodynamic product 9c, which has the CO trans to the pyridine nitrogen. The isomerization of 9t to 9c is shown not to take place via an associative mechanism and, with analogue 11, is effectively suppressed when excess chloride is added, implying that it takes place via a chloride dissociation. The monocyclometalated 9 undergoes a second cyclometalation to give the C boolean AND N boolean AND C dicyclometalated complex 15 in high yield. This second cyclometalation is brought about by the simple expedient of adding water to the monocyclometalated precursor. The addition of water is rationalized on the basis of needing to ionize the HCl byproduct of the reaction. Using a substituted pyridine (5) analogous chemistry is observed. Single-crystal X-ray structures of one of the intermediates (6) and one of the final products (15) have been solved. Density functional theory calculations are used to rationalize the isomerizations of the monocyclometalated intermediates and the need to ionize HCl in the second cyclometalation.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: ORGANOMETALLICS
Publisher: AMER CHEMICAL SOC
ISSN: 0276-7333
Date: 3 April 2000
Volume: 19
Number: 7
Number of Pages: 10
Page Range: pp. 1355-1364
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/13492

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us