Molecular models of site-isolated cobalt, rhodium, and iridium catalysts supported on zeolites: Ligand bond dissociation energies-Reference-Cited by-同舟云学术

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Molecular models of site-isolated cobalt, rhodium, and iridium catalysts supported on zeolites: Ligand bond dissociation energies

Published:2015-12 Issue: Volume:1074 Page:58-72
ISSN:2210-271X
Container-title:Computational and Theoretical Chemistry
language:en
Short-container-title:Computational and Theoretical Chemistry

Author:

Chen Mingyang,Serna Pedro,Lu Jing,Gates Bruce C.,Dixon David A.

Funder

Chemical Sciences, Geosciences, and Biosciences Division, Office of Basic Energy Sciences, U.S. Department of Energy

The University of Alabama

Oak Ridge Leadership Computing Facility at the Oak Ridge National Laboratory

Office of Science of the U.S. Department of Energy

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry

Reference60 articles.

1. 129Xe NMR spectroscopy of metal carbonyl clusters and metal clusters in zeolite NaY;Labouriau;J. Am. Chem. Soc.,1999

2. Size-dependent catalytic activity of zeolite-supported iridium clusters;Li;J. Phys. Chem. C,2007

3. Molecular chemistry in a zeolite: genesis of a zeolite Y-supported ruthenium complex catalyst;Ogino;J. Am. Chem. Soc.,2008

4. Transient spectroscopic characterization of the genesis of a ruthenium complex catalyst supported on zeolite Y;Ogino;J. Phys. Chem. C,2009

5. Reactions of highly uniform zeolite H-β-supported rhodium complexes: transient characterization by infrared and X-ray absorption spectroscopies;Ogino;J. Phys. Chem. C,2010

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