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Alkyl scandium complexes coordinated by dianionic O,N,N- and O,N,O-ligands derived from Schiff bases

Galina Andreevna Gurina 1
Galina Andreevna Gurina
Alexander Andreevich Kissel 2
Alexander Andreevich Kissel
Anatoly Mikhailovich Ob'edkov 1
Anatoly Mikhailovich Ob'edkov
Vladimir Kuzmich Cherkasov 1
Vladimir Kuzmich Cherkasov
Aleksandr Anatol'evich Trifonov
Published 2021-09-08
CommunicationVolume 31, Issue 5, 631-634
5
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Gurina G. A. et al. Alkyl scandium complexes coordinated by dianionic O,N,N- and O,N,O-ligands derived from Schiff bases // Mendeleev Communications. 2021. Vol. 31. No. 5. pp. 631-634.
GOST all authors (up to 50) Copy
Gurina G. A., Kissel A. A., Ob'edkov A. M., Cherkasov V. K., Trifonov A. A. Alkyl scandium complexes coordinated by dianionic O,N,N- and O,N,O-ligands derived from Schiff bases // Mendeleev Communications. 2021. Vol. 31. No. 5. pp. 631-634.
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TY - JOUR
DO - 10.1016/j.mencom.2021.09.013
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.09.013
TI - Alkyl scandium complexes coordinated by dianionic O,N,N- and O,N,O-ligands derived from Schiff bases
T2 - Mendeleev Communications
AU - Gurina, Galina Andreevna
AU - Kissel, Alexander Andreevich
AU - Ob'edkov, Anatoly Mikhailovich
AU - Cherkasov, Vladimir Kuzmich
AU - Trifonov, Aleksandr Anatol'evich
PY - 2021
DA - 2021/09/08
PB - Mendeleev Communications
SP - 631-634
IS - 5
VL - 31
ER -
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@article{2021_Gurina,
author = {Galina Andreevna Gurina and Alexander Andreevich Kissel and Anatoly Mikhailovich Ob'edkov and Vladimir Kuzmich Cherkasov and Aleksandr Anatol'evich Trifonov},
title = {Alkyl scandium complexes coordinated by dianionic O,N,N- and O,N,O-ligands derived from Schiff bases},
journal = {Mendeleev Communications},
year = {2021},
volume = {31},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.09.013},
number = {5},
pages = {631--634},
doi = {10.1016/j.mencom.2021.09.013}
}
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Gurina, Galina Andreevna, et al. “Alkyl scandium complexes coordinated by dianionic O,N,N- and O,N,O-ligands derived from Schiff bases.” Mendeleev Communications, vol. 31, no. 5, Sep. 2021, pp. 631-634. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2021.09.013.

Keywords

alkyl complexes
catalysis
dehydrocoupling
hydrophosphination
organophosphorus compounds
organosilicon compounds
scandium

Abstract

The reactions of imino phenols 3,5-But2-2-HOC6H2CH=NX (X = 8-C9H6N, 2-MeO-5-MeC6H3 and 2-PhOC6H4) with Sc(CH2SiMe3)3(THF)2 in toluene proceed with silane elimination and reductive alkylation of the C=N group affording dimeric base-free monoalkyl scandium complexes. X-ray analysis of the two complexes revealed their dimeric structures due to μ-bridging amidophenolato dianions. The complexes catalyze hydrophosphination of styrene, phenylacetylene and tolane with Ph2PH as well as dehydrogenative coupling of anisole with hydrosilanes.

References

3.
A quarter-century long story of bis(alkyl) rare-earth (III) complexes
Trifonov A.A., Lyubov D.M.
Coordination Chemistry Reviews, 2017
4.
Homoleptic Rare-Earth Metal Complexes Containing Ln−C σ-Bonds
5.
Synthesis of Chiral Aminocyclopropanes by Rare-Earth-Metal-Catalyzed Cyclopropene Hydroamination
Teng H., Luo Y., Wang B., Zhang L., Nishiura M., Hou Z.
Angewandte Chemie - International Edition, 2016
6.
10.1016/j.mencom.2021.09.013_b0030
Arndt
Chem. Rev., 1953
7.
10.1016/j.mencom.2021.09.013_b0035
Li
Applied Homogeneous Catalysis with Organometallic Compounds, 2017
9.
Cationic Organometallic Complexes of Scandium, Yttrium, and the Lanthanoids
Zeimentz P.M., Arndt S., Elvidge B.R., Okuda J.
Chemical Reviews, 2006
11.
Rare-earth metal complexes as catalysts for ring-opening polymerization of cyclic esters
Lyubov D.M., Tolpygin A.O., Trifonov A.A.
Coordination Chemistry Reviews, 2019
13.
Stereocontrolled ring-opening polymerisation of lactide
Stanford M.J., Dove A.P.
Chemical Society Reviews, 2010
15.
CH Bond Activation by f‐Block Complexes
Arnold P.L., McMullon M.W., Rieb J., Kühn F.E.
Angewandte Chemie - International Edition, 2014
16.
Rare-Earth-Catalyzed C–H Bond Addition of Pyridines to Olefins
Guan B., Hou Z.
Journal of the American Chemical Society, 2011
18.
σ-Bond Metathesis: A 30-Year Retrospective
19.
Energy materials based on metal Schiff base complexes
Zhang J., Xu L., Wong W.
Coordination Chemistry Reviews, 2018
21.
Catalytic activities of Schiff base transition metal complexes
Gupta K.C., Sutar A.K.
Coordination Chemistry Reviews, 2008
23.
Lanthanides: Schiff base complexes, applications in cancer diagnosis, therapy, and antibacterial activity
Kaczmarek M.T., Zabiszak M., Nowak M., Jastrzab R.
Coordination Chemistry Reviews, 2018
27.
Synthesis, structure and catalytic activity of new iminophenolato complexes of scandium and yttrium
Lara-Sanchez A., Rodriguez A., Hughes D.L., Schormann M., Bochmann M.
Journal of Organometallic Chemistry, 2002
29.
Synthesis, structure, and catalytic activity of organolanthanide complexes with chiral biaryl Schiff-base ligands
32.
Migration of amide to imine group of lanthanide Schiff base complexes: effect of amido group
33.
10.1016/j.mencom.2021.09.013_b0165
Cui
Sci. Technol., 2014
34.
Organometallic Complexes of Scandium and Yttrium Supported by a Bulky Salicylaldimine Ligand
Emslie D.J., Piers W.E., Parvez M., McDonald R.
Organometallics, 2002
36.
Scandium SALEN Complexes Bearing Chloro, Aryloxo, and Hydroxo Ligands
Meermann C., Törnroos K.W., Anwander R.
Inorganic Chemistry, 2009
39.
Tables of bond lengths determined by X-ray and neutron diffraction. Part 1. Bond lengths in organic compounds
Allen F.H., Kennard O., Watson D.G., Brammer L., Orpen A.G., Taylor R.
Journal of the Chemical Society Perkin Transactions 2, 1987
40.
10.1016/j.mencom.2021.09.013_b0200
Yacobi
Semiconductor Materials: An Introduction to Basic Principles (Microdevices), 2013
41.
Organosilicon Chemistry VI: From Molecules to Materials, eds. N. Auner and J. Weis, Wiley-VCH, 2008.
42.
10.1016/j.mencom.2021.09.013_b0210
Rösch
Wiley-VCH, 2000
43.
Organosilicon Biotechnology
Frampton M.B., Zelisko P.M.
Silicon, 2009
44.
Progress in the medicinal chemistry of silicon: C/Si exchange and beyond
45.
Organosilicon Molecules with Medicinal Applications
Franz A.K., Wilson S.O.
Journal of Medicinal Chemistry, 2012
46.
Selective C–Si Bond Formation through C–H Functionalization
Sharma U., Sharma R., Kumar R., Kumar I., Singh B.
Synthesis, 2015
48.
Scandium-Catalyzed Silylation of Aromatic CH Bonds
Oyamada J., Nishiura M., Hou Z.
Angewandte Chemie - International Edition, 2011
49.
Bruker APEX3, SAINT, Bruker AXS, Madison, WI, 2018.
50.
CrysAlisPro 1.171.38.46, Rigaku Oxford Diffraction, Rigaku Corporation, Wroclaw, Poland, 2018.
51.
SHELXT– Integrated space-group and crystal-structure determination
Sheldrick G.M.
Acta Crystallographica Section A: Foundations and Advances, 2015
52.
Comparison of silver and molybdenum microfocus X-ray sources for single-crystal structure determination
Krause L., Herbst-Irmer R., Sheldrick G.M., Stalke D.
Journal of Applied Crystallography, 2015