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Cited by 317

The DOI matches its Crossref record; 72 of the 72 references it cites were found in a registry or an index.

Mechanistic Studies on the Reversible Hydrogenation of Carbon Dioxide Catalyzed by an Ir-PNP Complex

Tanaka, Ryo, Yamashita, Makoto, Chung, Lung Wa, Morokuma, Keiji, Nozaki, Kyoko·2011·Organometallics

Abstract

The PNP-ligated iridium(III) trihydride complex 1 exhibited the highest catalytic activity for hydrogenation of carbon dioxide in aqueous KOH. The catalytic hydrogenation can be tuned to be a reversible process with the same catalyst at the expense of the activity, when triethanolamine was used as a base. Theoretical studies on the hydrogenation of carbon dioxide using DFT calculations suggested two competing reaction pathways: either the deprotonative dearomatization step or the hydrogenolysis step as the rate-determining step. The results nicely explain our experimental observations that the catalytic cycle is dependent on both the strength of the base and hydrogen pressure.

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Metadata

Authors
Tanaka, R., Yamashita, M., Chung, L. W., Morokuma, K., & Nozaki, K.
Venue
Organometallics
Published
2011-11-30
Volume
30
Issue
24
Pages
6742-6750
ISSN
  • 0276-7333 (ISSN-L)
  • 1520-6041
OpenAlex
W2324462072
Cited by
317
References
72
FWCI
10.37
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Mechanistic Studies on the Reversible Hydrogenation of Carbon Dioxide Catalyzed by an Ir-PNP Complex. https://app.cochat.ai/papers/10.1021/om2010172
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Tanaka, R., Yamashita, M., Chung, L. W., Morokuma, K., & Nozaki, K. (2011). Mechanistic Studies on the Reversible Hydrogenation of Carbon Dioxide Catalyzed by an Ir-PNP Complex. Organometallics. https://doi.org/10.1021/om2010172

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