Physical insights into mechanistic processes in organometallic chemistry: an introduction

被引:3
|
作者
Morris, Robert H. [1 ]
机构
[1] Univ Taranto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ASYMMETRIC TRANSFER HYDROGENATION; NEUTRAL-LIGAND COMPLEXES; BIS(IMINO)PYRIDINE IRON; ELECTRONIC-STRUCTURE; PRESSURE HYDROGENATION; CATALYSTS; KETONES; DEHYDROGENATION; ALCOHOLS; REDUCTION;
D O I
10.1039/c9fd00083f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The challenges of research into the mechanisms of 4d versus 3d late transition metal homogeneous catalysts is considered here, particularly catalysts containing hydrides. Included are case studies of C-H bond activation as studied in a collaboration of the Weller and McIndoe groups where a ruthenium (4d) hydride intermediate is detected using ESI-MS analysis of the catalytic mixture, and as studied in a collaboration of the Thomas and Neidig groups where a hydride transfer step involving low valent iron (3d) catalytic species is investigated using low temperature methods including Mossbauer spectroscopy. In the asymmetric hydrogenation of olefins, mechanisms are considered for rhodium (4d) vs. the newly discovered cobalt (3d) metal catalysts from the Shevlin and Chirik groups. The Hintermair group has recently described a study of a Noyori ruthenium catalyst for the ATH of acetophenone in basic 2-PrOH using a variety of flow sampling methods including flow NMR. This mechanism is highlighted along with our iron hydride work in homogeneous asymmetric hydrogenation.
引用
收藏
页码:10 / 27
页数:18
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