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Synthesis, reactivity, and catalytic application of tetraphenylcyclobutadiene iridium complexes

Nikita Vyacheslavovich Shvydkiy 1
Nikita Vyacheslavovich Shvydkiy
Yulia Vladimirovna Nelyubina 1
Yulia Vladimirovna Nelyubina
1 A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Published 2024-06-19
CommunicationVolume 34, Issue 4, 547-549
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Shvydkiy N. V., Nelyubina Y. V., Perekalin D. S. Synthesis, reactivity, and catalytic application of tetraphenylcyclobutadiene iridium complexes // Mendeleev Communications. 2024. Vol. 34. No. 4. pp. 547-549.
GOST all authors (up to 50) Copy
Shvydkiy N. V., Nelyubina Y. V., Perekalin D. S. Synthesis, reactivity, and catalytic application of tetraphenylcyclobutadiene iridium complexes // Mendeleev Communications. 2024. Vol. 34. No. 4. pp. 547-549.
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TY - JOUR
DO - 10.1016/j.mencom.2024.06.025
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2024.06.025
TI - Synthesis, reactivity, and catalytic application of tetraphenylcyclobutadiene iridium complexes
T2 - Mendeleev Communications
AU - Shvydkiy, Nikita Vyacheslavovich
AU - Nelyubina, Yulia Vladimirovna
AU - Perekalin, Dmitrii Sergeevich
PY - 2024
DA - 2024/06/19
PB - Mendeleev Communications
SP - 547-549
IS - 4
VL - 34
ER -
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@article{2024_Shvydkiy,
author = {Nikita Vyacheslavovich Shvydkiy and Yulia Vladimirovna Nelyubina and Dmitrii Sergeevich Perekalin},
title = {Synthesis, reactivity, and catalytic application of tetraphenylcyclobutadiene iridium complexes},
journal = {Mendeleev Communications},
year = {2024},
volume = {34},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2024.06.025},
number = {4},
pages = {547--549},
doi = {10.1016/j.mencom.2024.06.025}
}
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Shvydkiy, Nikita Vyacheslavovich, et al. “Synthesis, reactivity, and catalytic application of tetraphenylcyclobutadiene iridium complexes.” Mendeleev Communications, vol. 34, no. 4, Jun. 2024, pp. 547-549. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2024.06.025.

Keywords

cyclobutadiene
diazo compounds.
diene ligands
homogeneous catalysis
iridium

Abstract

Reaction of [(coe)2IrCl]2 (coe = cyclooctene) with AgPF6, arene (toluene, p-xylene, mesitylene), and diphenylacetylene, followed by counter anion exchange to BARF-, gives cyclobutadiene iridium complexes [(C4Ph4)Ir(arene)]BARF in 10-22% yield. Replacement of toluene in [(C4Ph4)Ir(toluene)]BARF by various ligands (trimethyl-phosphite, 1,3,5-triaza-7-phosphaadamantane, tert-butyl isonitrile) provides access to the half-sandwich cyclobuta-diene iridium complexes [(C4Ph4)Ir(L)3]BARF. Complex [(C4Ph4)Ir(toluene)]BARF in combination with [NBnEt3]Cl catalyses the insertion reaction between phenyl diazoacetate and various amines.

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