Phosphine-substituted Fe–Te clusters related to the active site of [FeFe]-H2ases-Reference-Cited by-同舟云学术

Phosphine-substituted Fe–Te clusters related to the active site of [FeFe]-H2ases

Published:2020 Issue:12 Volume:7 Page:2352-2361
ISSN:2052-1553
Container-title:Inorganic Chemistry Frontiers
language:en
Short-container-title:Inorg. Chem. Front.

Author:

Lü Shuang¹²³⁴,Huang Hong-Li⁵⁶²⁷⁴,Zhang Ru-fen⁵⁶²⁷⁴,Ma Chun-lin⁵⁶²⁷⁴^ORCID,Li Qian-Li⁵⁶²⁷⁴^ORCID,He Jiao⁸⁹¹⁰⁴,Yang Jun⁸⁹¹⁰⁴,Li Ting⁸⁹¹⁰⁴,Li Yu-Long⁸⁹¹⁰⁴¹¹^ORCID

Affiliation:

1. School of Pharmacy

2. Liaocheng University

3. Liaocheng 252059

4. P.R. China

5. Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology

6. College of Chemistry and Chemical Engineering

7. Liaocheng

8. College of Chemistry and Environmental Engineering

9. Sichuan University of Science & Engineering

10. Zigong 643000

11. Chemical Synthesis and Pollution Control Key Laboratory of Sichuan Province

Abstract

Mono-, di-, and tetranuclear phosphine-substituted Fe/Te clusters 1–6 were described.

Funder

Natural Science Foundation of Shandong Province

National Natural Science Foundation of China

Sichuan University of Science and Engineering

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QI/D0QI00276C

Reference53 articles.

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2. Synthesis of Diiron(I) Dithiolato Carbonyl Complexes

3. Synthetic and Structural Studies of [FeFe]-Hydrogenase Models Containing a Butterfly Fe/E (E = S, Se, or Te) Cluster Core. Electrocatalytic H2 Evolution Catalyzed by [(μ-SeCH2)(μ-CH2NCH2Ph)]Fe2(CO)6

4. Hydrogenases

5. X-ray Crystal Structure of the Fe-Only Hydrogenase (CpI) from Clostridium pasteurianum to 1.8 Angstrom Resolution

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