Multidentate Phosphanyl Phosphinines: Synthesis and Properties-Reference-Cited by-同舟云学术

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Multidentate Phosphanyl Phosphinines: Synthesis and Properties

Published:2018-05-15 Issue:33 Volume:24 Page:8432-8437
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Chen Xiaodan¹,Li Zhongshu²^ORCID,Grützmacher Hansjörg²³

Affiliation:

1. College of Chemistry and Materials Science; Jinan University; 510632 Guangzhou P.R. China

2. Lehn Institute of Functional Materials (LIFM); School of Chemistry; Sun Yat-Sen University 510275 Guangzhou P.R. China

3. Department of Chemistry and Applied Biosciences; ETH Zurich; 8093 Zurich Switzerland

Funder

National Natural Science Foundation of China

Fundamental research funds of Central Universities

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference74 articles.

1. 2,4,6-Triphenylphosphabenzol

2. Phosphabenzene and arsabenzene

3. Temporary anion states of phosphabenzene, arsabenzene, and stibabenzene. Trends in the .pi. and .pi.* orbital energies

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Diphosphene with a phosphineborane tether and its rhodium complex;Dalton Transactions;2024

2. Highly selective, reversible water activation by P,N-cooperativity in pyridyl-functionalized phosphinines;Chemical Science;2024

3. The case of a μ₂-P aromatic phosphinine as a 4-electron donor forming σ- and π-three–center-two-electron bonds;Dalton Transactions;2024

4. Phosphinine vs Pyridine in Luminescent Cu^I Complexes and Application in Lifetime‐Based Molecular Thermometer;European Journal of Inorganic Chemistry;2023-10-26

5. Understanding the Mechanism of Diels–Alder Reactions with Anionic Dienophiles: A Systematic Comparison of [ECX]⁻ (E = P, As; X = O, S, Se) Anions;Inorganic Chemistry;2022-05-09

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