CO2 hydrogenation by phosphorus-nitrogen PN3P-pincer iridium hydride complexes: elucidation of the deactivation pathway.

Yupeng Pan; Chao Guan; Huaifeng Li; Priyanka Chakraborty; Chunhui Zhou; Kuo-Wei Huang

doi:10.1039/c9dt01319a

CO2 hydrogenation by phosphorus-nitrogen PN3P-pincer iridium hydride complexes: elucidation of the deactivation pathway.

Yupeng Pan, Chao Guan, Huaifeng Li, Priyanka Chakraborty, Chunhui Zhou, Kuo-Wei Huang

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

PN3P-Ir pincer hydride complexes were synthesized and characterized as catalysts and key intermediates in the direct hydrogenation of CO2 to formate under mild conditions. The formation of a dearomatized PN3P*-Ir(i)-CO species was identified as a plausible key process accountable for the loss of catalytic activity in the CO2 hydrogenation.

Original language	English (US)
Pages (from-to)	12812-12816
Number of pages	5
Journal	Dalton transactions (Cambridge, England : 2003)
Volume	48
Issue number	34
DOIs	https://doi.org/10.1039/c9dt01319a
State	Published - 2019

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title = "CO2 hydrogenation by phosphorus-nitrogen PN3P-pincer iridium hydride complexes: elucidation of the deactivation pathway.",

abstract = "PN3P-Ir pincer hydride complexes were synthesized and characterized as catalysts and key intermediates in the direct hydrogenation of CO2 to formate under mild conditions. The formation of a dearomatized PN3P*-Ir(i)-CO species was identified as a plausible key process accountable for the loss of catalytic activity in the CO2 hydrogenation.",

author = "Yupeng Pan and Chao Guan and Huaifeng Li and Priyanka Chakraborty and Chunhui Zhou and Kuo-Wei Huang",

note = "KAUST Repository Item: Exported on 2020-10-01 Acknowledgements: This work was supported by funding from the King Abdullah University of Science and Technology (KAUST).",

year = "2019",

doi = "10.1039/c9dt01319a",

language = "English (US)",

volume = "48",

pages = "12812--12816",

journal = "Dalton transactions (Cambridge, England : 2003)",

issn = "1477-9226",

publisher = "Royal Society of Chemistry",

number = "34",

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CO2 hydrogenation by phosphorus-nitrogen PN3P-pincer iridium hydride complexes: elucidation of the deactivation pathway. / Pan, Yupeng; Guan, Chao; Li, Huaifeng; Chakraborty, Priyanka; Zhou, Chunhui; Huang, Kuo-Wei.

In: Dalton transactions (Cambridge, England : 2003), Vol. 48, No. 34, 2019, p. 12812-12816.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - CO2 hydrogenation by phosphorus-nitrogen PN3P-pincer iridium hydride complexes: elucidation of the deactivation pathway.

AU - Pan, Yupeng

AU - Guan, Chao

AU - Li, Huaifeng

AU - Chakraborty, Priyanka

AU - Zhou, Chunhui

AU - Huang, Kuo-Wei

N1 - KAUST Repository Item: Exported on 2020-10-01 Acknowledgements: This work was supported by funding from the King Abdullah University of Science and Technology (KAUST).

PY - 2019

Y1 - 2019

N2 - PN3P-Ir pincer hydride complexes were synthesized and characterized as catalysts and key intermediates in the direct hydrogenation of CO2 to formate under mild conditions. The formation of a dearomatized PN3P*-Ir(i)-CO species was identified as a plausible key process accountable for the loss of catalytic activity in the CO2 hydrogenation.

AB - PN3P-Ir pincer hydride complexes were synthesized and characterized as catalysts and key intermediates in the direct hydrogenation of CO2 to formate under mild conditions. The formation of a dearomatized PN3P*-Ir(i)-CO species was identified as a plausible key process accountable for the loss of catalytic activity in the CO2 hydrogenation.

UR - http://hdl.handle.net/10754/656480

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UR - http://www.scopus.com/inward/record.url?scp=85071641250&partnerID=8YFLogxK

U2 - 10.1039/c9dt01319a

DO - 10.1039/c9dt01319a

M3 - Article

C2 - 31402365

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SP - 12812

EP - 12816

JO - Dalton transactions (Cambridge, England : 2003)

JF - Dalton transactions (Cambridge, England : 2003)

SN - 1477-9226

IS - 34

ER -

CO2 hydrogenation by phosphorus-nitrogen PN3P-pincer iridium hydride complexes: elucidation of the deactivation pathway.

Abstract

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