Origin of Bonding Interactions in Cu+(H2)n Clusters: An Experimental and Theoretical Investigation-Reference-Cited by-同舟云学术

Origin of Bonding Interactions in Cu+(H2)n Clusters: An Experimental and Theoretical Investigation

Published:1998-12-01 Issue:51 Volume:120 Page:13494-13502
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kemper Paul R.¹,Weis Patrick¹,Bowers Michael T.¹,Maître Philippe¹

Affiliation:

1. Contribution from the Department of Chemistry, The University of California at Santa Barbara, Santa Barbara, California 93106-9510, and Laboratoire de Chimie Théorique, Université de Paris-Sud, Centre d'Orsay, 91405 Orsay Cedex

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9822658

Reference44 articles.

1. Characterization of the first examples of isolable molecular hydrogen complexes, M(CO)3(PR3)2(H2) (M = molybdenum or tungsten; R = Cy or isopropyl). Evidence for a side-on bonded dihydrogen ligand

2. Insertion of Sc+ into H2: The First Example of Cluster-Mediated .sigma.-Bond Activation by a Transition Metal Center

3. Binding energies of Ti+(H2)1–6 clusters: Theory and experiment

4. Spin change induced in vanadium(I) by low-field ligands: binding energies of vanadium ion-hydrogen (V+(H2)n) clusters (n = 1-7)

5. Cr+(H2)n clusters: Asymmetric bonding from a symmetric ion

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