Calcium Hydride Cation Dimer Catalyzed Hydrogenation of Unactivated 1‐Alkenes and H2 Isotope Exchange: Competitive Ca−H−Ca Bridges and Terminal Ca−H Bonds
Recently, it was shown that the double Ca−H−Ca bridged calcium hydride cation dimer complex [LCaH2CaL]2+ (macrocyclic ligand L=NNNN‐tetradentate Me4TACD) exhibited remarkable activity in catalyzing the hydrogenation of unactivated 1‐alkenes as well as the H2 isotope exchange under mild conditions, t...
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Published in | Chemistry : a European journal Vol. 29; no. 1; pp. e202202602 - n/a |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Wiley Subscription Services, Inc
02.01.2023
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Recently, it was shown that the double Ca−H−Ca bridged calcium hydride cation dimer complex [LCaH2CaL]2+ (macrocyclic ligand L=NNNN‐tetradentate Me4TACD) exhibited remarkable activity in catalyzing the hydrogenation of unactivated 1‐alkenes as well as the H2 isotope exchange under mild conditions, tentatively via the terminal Ca−H bond of cation monomer LCaH+. In this DFT mechanistic work, a novel substrate‐dependent catalytic mechanism is disclosed involving cooperative Ca−H−Ca bridges for H2 isotope exchange, competitive Ca−H−Ca bridges and terminal Ca−H bonds for anti‐Markovnikov addition of unactivated 1‐alkenes, and terminal Ca−H bonds for Markovnikov addition of conjugation‐activated styrene. THF‐coordination plays a key role in favoring the anti‐Markovnikov addition while strong cation‐π interactions direct the Markovnikov addition to terminal Ca−H bonds.
Calcium hydride cation dimer catalysis: Dispersion‐corrected DFT calculations reveal that the same double Ca−H−Ca bridged calcium hydride cation dimer catalyst [LCaH2CaL]2+⋅THF shows a novel substrate‐dependent catalytic activity, involving cooperative Ca−H−Ca bridges for efficient H2 isotope exchange, terminal Ca−H bond for the Markovnikov addition of conjugation‐activated styrene, and competitive Ca−H−Ca bridges and terminal Ca−H bonds for the anti‐Markovnikov addition of unactivated 1‐alkenes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0947-6539 1521-3765 1521-3765 |
DOI: | 10.1002/chem.202202602 |