Calculated Hydride Donor Abilities of Five-Coordinate Transition Metal Hydrides [HM(diphosphine)2]+ (M = Ni, Pd, Pt) as a Function of the Bite Angle and Twist Angle of Diphosphine Ligands-Reference-Cited by-同舟云学术

Calculated Hydride Donor Abilities of Five-Coordinate Transition Metal Hydrides [HM(diphosphine)2]+ (M = Ni, Pd, Pt) as a Function of the Bite Angle and Twist Angle of Diphosphine Ligands

Published:2008-05-17 Issue:12 Volume:27 Page:2715-2722
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Nimlos Mark R.¹,Chang Christopher H.¹,Curtis Calvin J.¹,Miedaner Alex¹,Pilath Heidi M.¹,DuBois Daniel L.¹

Affiliation:

1. National Renewable Energy Laboratory, Golden, Colorado 80401, and Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om701218x

Reference49 articles.

1. Crystallographic and FTIR Spectroscopic Evidence of Changes in Fe Coordination Upon Reduction of the Active Site of the Fe-Only Hydrogenase from Desulfovibrio desulfuricans

2. X-ray Crystal Structure of the Fe-Only Hydrogenase (CpI) from Clostridium pasteurianum to 1.8 Angstrom Resolution

3. Mössbauer Characterization of the Iron−Sulfur Clusters in Desulfovibrio vulgaris Hydrogenase

4. Removal of the bridging ligand atom at the Ni–Fe active site of [NiFe] hydrogenase upon reduction with H2, as revealed by X-ray structure analysis at 1.4 Å resolution

5. The active site and catalytic mechanism of NiFe hydrogenases

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