Research output: Contribution to journal › Article › peer-review
Reaction of coordinated isocyanides with substituted N -(2-pyridyl) ureas as a route to new cyclometallated Pd(II) complexes. / Geyl, Kirill K. ; Baykov, Sergey V. ; Kasatkina, Svetlana O. ; Savko, Polina Yu. ; Boyarskiy, Vadim P. .
In: Journal of Organometallic Chemistry, Vol. 980-981, 122518, 01.12.2022.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Reaction of coordinated isocyanides with substituted N -(2-pyridyl) ureas as a route to new cyclometallated Pd(II) complexes
AU - Geyl, Kirill K.
AU - Baykov, Sergey V.
AU - Kasatkina, Svetlana O.
AU - Savko, Polina Yu.
AU - Boyarskiy, Vadim P.
N1 - Publisher Copyright: © 2022
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Substituted N-(pyridin-2-yl) ureas or carbamates act as polynucleophiles upon the reaction with palladium(II) bis(isocyanide) complexes at RT to give metallacycles containing azaheterocyclic and urea fragments. Nine new C,N-chelate deprotonated diaminocarbene palladium(II) complexes were synthesized by coupling substituted N-(2-pyridyl)ureas and coordinated isocyanides. The obtained yellow or green-yellow species were characterized by high-resolution mass spectrometry and 1D (1H, 13C) NMR spectroscopies. The structures of six complexes in a solid state were elucidated by single-crystal X-ray diffraction (XRD). This universal and convenient method for the preparation of C^N-cyclometallated palladium(II) complexes under mild conditions opens the way to the targeted synthesis of polyfunctional organometallic compounds that combine the chemical, biological, and photophysical properties of metallacycles and parent azaheterocycles.
AB - Substituted N-(pyridin-2-yl) ureas or carbamates act as polynucleophiles upon the reaction with palladium(II) bis(isocyanide) complexes at RT to give metallacycles containing azaheterocyclic and urea fragments. Nine new C,N-chelate deprotonated diaminocarbene palladium(II) complexes were synthesized by coupling substituted N-(2-pyridyl)ureas and coordinated isocyanides. The obtained yellow or green-yellow species were characterized by high-resolution mass spectrometry and 1D (1H, 13C) NMR spectroscopies. The structures of six complexes in a solid state were elucidated by single-crystal X-ray diffraction (XRD). This universal and convenient method for the preparation of C^N-cyclometallated palladium(II) complexes under mild conditions opens the way to the targeted synthesis of polyfunctional organometallic compounds that combine the chemical, biological, and photophysical properties of metallacycles and parent azaheterocycles.
KW - C^N-cyclometallated complexes
KW - Palladium(II)
KW - isocyanides
KW - Ureas
KW - heterocycles
KW - Heterocycles
KW - Isocyanides
UR - http://www.scopus.com/inward/record.url?scp=85138535240&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/d86ce44a-2815-39de-be56-0296ca81b2ec/
U2 - 10.1016/j.jorganchem.2022.122518
DO - 10.1016/j.jorganchem.2022.122518
M3 - Article
VL - 980-981
JO - Journal of Organometallic Chemistry
JF - Journal of Organometallic Chemistry
SN - 0022-328X
M1 - 122518
ER -
ID: 99947819