Elliott L. Blinn, and Ralph G. Wilkins .... Michael J. Blandamer , John Burgess , Diane L. Elvidge , Pilar Guardado , Andrew W. Hakin , Lesley J. S. P...
Nov 1, 1976 - Elliott L. Blinn, Ralph G. Wilkins ... Eric S. Okerberg , Said Elshihabi , Peter T. Carmichael , Kathryn A. Woody , Timothy A. Barckholtz , John A.
Apr 30, 1976 - Mechanisms of Racemization of M(phen)32+ Ions. AIC60316P. Sir: A fewyears ago Sutter and Hunt1 reported that Cr-. (phen)32+ (phen =.
Elliott L. Blinn, and Ralph G. Wilkins. Inorg. ... Eric S. Okerberg , Said Elshihabi , Peter T. Carmichael , Kathryn A. Woody , Timothy A. Barckholtz , John A. Burke ...
Nov 1, 1982 - ... Terence A. Nile, and Jerry L. Walsh , David W. Thompson and John D. ... Youxiang Wang, Willie J. Perez, Greg Y. Zheng, D. Paul Rillema, ...
Electronic Spectra of Tris(2,2â²-bipyridine)-M(II) Complex Ions in Vacuo (M = Fe and Os) ... Stephanie Bellinger-Buckley , Tse-Cing Chang , Seema Bag , David Schweinfurth ... The Journal of Physical Chemistry B 2013 117 (12), 3428-3438 ... Benjamin
Chandima Abeywickrama and Arthur David Baker. The Journal of Organic Chemistry 2004 69 (22), 7741-7744. Abstract | Full Text HTML | PDF | PDF w/ Links.
Jan 22, 2010 - The Stöber method,(16) in which tetraethoxysilane (TEOS) was used as silica source and ammonia as catalyst, is the most widely adopted ...
A. David Baker, Robert J. Morgan, and Thomas C. Strekas. J. Am. Chem. ... Chris M. Shelton, Kathryn E. Seaver, John F. Wheeler, and Noel A. P. Kane-Maguire.
May 18, 1990 - A. David Baker, Robert J. Morgan, and Thomas C. Strekas*. Department of Chemistry and Biochemistry. Queens College of the City University ...
Correspondence Table I. R a t e Parameters for Ligand Dissociation and Racemization of M(phen)," Ions at 25 "C
Mechanisms of Racemization of M(phen)3?+ Ions AIC603 16P
Sir: A few years ago Sutter and Hunt' reported that Cr( ~ h e n ) 3 ~ "(phen = 1,lo-phenanthroline) reacted with ( + ) ~ - C o ( p h e n ) 3 ~to+ yield (-)~-Cr(phen)3~+ and that when (-)~-Co(phen)3~+ was the reactant (+)~-Cr(phen)3~+ resulted. There was thus indicated a substantial (84%) stereospecificity in this outer-sphere redox reaction. The observations demanded additionally that the (rapid) redox reaction must be much slower than the inversion of C r ( ~ h e n ) 3 ~so + , as to allow the optical form of C r ( ~ h e n ) 3 ~which + is oxidized more rapidly by C0(phen)3~+to be continuously regenerated. This required a racemization half-life
