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First example of a click-reaction on the aminate copper complexes: effect of reaction parameters

Igor Vladimirovich Esarev 1
Igor Vladimirovich Esarev
Vladislav V Gurzhiy 2
Vladislav V Gurzhiy
Artem Alexandrovich Selyutin 2
Artem Alexandrovich Selyutin
Anastasia Vladimirovna Laptenkova 2
Anastasia Vladimirovna Laptenkova
Andrey Igorevich Poddel'sky 3
Andrey Igorevich Poddel'sky
Nicolay Leonidovich Medvedskiy 1
Nicolay Leonidovich Medvedskiy
Alexander Ivanovich Ponyaev 1
Alexander Ivanovich Ponyaev
Rostislav Evgen'evich Trifonov 1, 2
Rostislav Evgen'evich Trifonov
Alexey Vladimirovich Eremin 1, 4
Alexey Vladimirovich Eremin
Published 2018-11-01
CommunicationVolume 28, Issue 6, 606-608
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Esarev I. V. et al. First example of a click-reaction on the aminate copper complexes: effect of reaction parameters // Mendeleev Communications. 2018. Vol. 28. No. 6. pp. 606-608.
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Esarev I. V., Gurzhiy V. V., Selyutin A. A., Laptenkova A. V., Poddel'sky A. I., Medvedskiy N. L., Ponyaev A. I., Trifonov R. E., Eremin A. V. First example of a click-reaction on the aminate copper complexes: effect of reaction parameters // Mendeleev Communications. 2018. Vol. 28. No. 6. pp. 606-608.
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TY - JOUR
DO - 10.1016/j.mencom.2018.11.014
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.014
TI - First example of a click-reaction on the aminate copper complexes: effect of reaction parameters
T2 - Mendeleev Communications
AU - Esarev, Igor Vladimirovich
AU - Gurzhiy, Vladislav V
AU - Selyutin, Artem Alexandrovich
AU - Laptenkova, Anastasia Vladimirovna
AU - Poddel'sky, Andrey Igorevich
AU - Medvedskiy, Nicolay Leonidovich
AU - Ponyaev, Alexander Ivanovich
AU - Trifonov, Rostislav Evgen'evich
AU - Eremin, Alexey Vladimirovich
PY - 2018
DA - 2018/11/01
PB - Mendeleev Communications
SP - 606-608
IS - 6
VL - 28
ER -
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@article{2018_Esarev,
author = {Igor Vladimirovich Esarev and Vladislav V Gurzhiy and Artem Alexandrovich Selyutin and Anastasia Vladimirovna Laptenkova and Andrey Igorevich Poddel'sky and Nicolay Leonidovich Medvedskiy and Alexander Ivanovich Ponyaev and Rostislav Evgen'evich Trifonov and Alexey Vladimirovich Eremin},
title = {First example of a click-reaction on the aminate copper complexes: effect of reaction parameters},
journal = {Mendeleev Communications},
year = {2018},
volume = {28},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.014},
number = {6},
pages = {606--608},
doi = {10.1016/j.mencom.2018.11.014}
}
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Esarev, Igor Vladimirovich, et al. “First example of a click-reaction on the aminate copper complexes: effect of reaction parameters.” Mendeleev Communications, vol. 28, no. 6, Nov. 2018, pp. 606-608. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.014.

Abstract

The hydrothermal reaction of NaN3 with Cu(Phen)Cl2 in acetonitrile solutions results in the formation of two complexes: new d9 mononuclear cis-[CuII(Phen)2(mtz)2]·H2O and d10 coordination polymer catena-[CuI(Phen)(μ-CN)]n (mtz is 5-methyltetrazolate anion and Phen is 1,10-phenanthroline). The process involves in situ formation of mtz ligand via cycloaddition of acetonitrile and azide (in the case of [CuII(Phen)2(mtz)2]) and cleavage of acetonitrile C–C bond (in the case of [CuI(Phen)(μ-CN)]n). Both complexes were fully characterized by a comprehensive set of methods, including the single crystal X-ray diffraction data.

References

1.
10.1016/j.mencom.2018.11.014_bibe0010
Comprehensive Coordination Chemistry II, 2003
2.
Triazoles and tetrazoles: Prime ligands to generate remarkable coordination materials
Aromí G., Barrios L.A., Roubeau O., Gamez P.
Coordination Chemistry Reviews, 2011
3.
10.1016/j.mencom.2018.11.014_sbrefe0015b
Popova
Arkivoc, 2012
6.
Single-Walled Polytetrazolate Metal–Organic Channels with High Density of Open Nitrogen-Donor Sites and Gas Uptake
Lin Q., Wu T., Zheng S., Bu X., Feng P.
Journal of the American Chemical Society, 2011
8.
Metal–Organic Frameworks Based on Unprecedented Trinuclear and Pentanuclear Metal–Tetrazole Clusters as Secondary Building Units
9.
A new tetrazolate zeolite-like framework for highly selective CO2/CH4and CO2/N2separation
Xiong S., Gong Y., Wang H., Wang H., Liu Q., Gu M., Wang X., Chen B., Wang Z.
Chemical Communications, 2014
10.
A multicentre-bonded [ZnI]8 cluster with cubic aromaticity
Cui P., Hu H., Zhao B., Miller J.T., Cheng P., Li J.
Nature Communications, 2015
13.
Two Acentric Mononuclear Molecular Complexes with Unusual Magnetic and Ferroelectric Properties
Zhao F., Che Y., Zheng J., Grandjean F., Long G.J.
Inorganic Chemistry, 2012
14.
Multifunctionality in spin crossover materials
Gaspar A.B., Ksenofontov V., Seredyuk M., Gütlich P.
Coordination Chemistry Reviews, 2005
15.
Two Extended 5-Methyltetrazolate-Based Magnetic Complexes: Synthesis, Structure, and Magnetic Properties
Liu J., Dong H., Yang E., Zhao X.
Zeitschrift fur Anorganische und Allgemeine Chemie, 2013
16.
Synthesis of novel tetrazole derivatives and evaluation of their antifungal activity
Łukowska-Chojnacka E., Mierzejewska J., Milner-Krawczyk M., Bondaryk M., Staniszewska M.
Bioorganic and Medicinal Chemistry, 2016
17.
Synthesis, characterization and DNA cleavage studies of isomeric pyridyl-tetrazole ligands and their Ni(II) and Zn(II) complexes
Surendra Babu M.S., Rao B.U., Krishna V., Mustafa S., Rao G.N.
Journal of Saudi Chemical Society, 2017
18.
Developments in Tetrazole Chemistry (2009–16)
Ostrovskii V.A., Popova E.A., Trifonov R.E.
Advances in Heterocyclic Chemistry, 2017
19.
Preparation of 5-Substituted 1H-Tetrazoles from Nitriles in Water
Demko Z.P., Sharpless K.B.
Journal of Organic Chemistry, 2001
23.
Cu-free click cycloaddition reactions in chemical biology
Jewett J.C., Bertozzi C.R.
Chemical Society Reviews, 2010
26.
In Situ Tetrazole Ligand Synthesis of Two‐Fold Interpenetrating Zinc Coordination Frameworks
Ma L., Qiu Y., Peng G., Cai J., Deng H.
European Journal of Inorganic Chemistry, 2011
27.
Syntheses and coordination chemistry of perfluoroaryl-1H-tetrazoles
Gerhards H., Krest A., Eulgem P.J., Naumann D., Rokitta D., Valldor M., Klein A.
Polyhedron, 2015
30.
Carbon–carbon bond cleavage via oxidative addition: reaction of tetrakis(triphenylphosphine)platinum(0) with 1,1,1-tricyanoethane
Burmeister J.L., Edwards L.M.
Journal of the Chemical Society A Inorganic Physical Theoretical, 1971
31.
Synthesis, Structure and Photoluminescent Studies of a Novel Supramolecular [Ag(phen)(CN)]·(phen) Complex
Huang X., Zheng S., Zhang J., Chen X.
European Journal of Inorganic Chemistry, 2004
33.
C−C Bond Cleavage of Acetonitrile by a Dinuclear Copper(II) Cryptate
Lu T., Zhuang X., Li Y., Chen S.
Journal of the American Chemical Society, 2004
35.
Antimicrobial mechanism of copper (II) 1,10-phenanthroline and 2,2′-bipyridyl complex on bacterial and fungal pathogens
Chandraleka S., Ramya K., Chandramohan G., Dhanasekaran D., Priyadharshini A., Panneerselvam A.
Journal of Saudi Chemical Society, 2014
36.
Synthesis and Crystal Structures of Four Cyanide‐Bridged Coordination Polymers
He X., Lu C., Yuan D., Chen S., Chen J.
European Journal of Inorganic Chemistry, 2005
38.
10.1016/j.mencom.2018.11.014_bibe0095
Nie
Acta Crystallogr., 2010
39.
10.1016/j.mencom.2018.11.014_bibe0100
Shao
Acta Crystallogr., 2004
41.
5‐Cyanotetrazolate as a Ligand and Linker in Copper(II) Complexes and Coordination Polymers
42.
10.1016/j.mencom.2018.11.014_bibe0115
Zhang
Acta Crystallogr., 2007
43.
10.1016/j.mencom.2018.11.014_bibe0120
Huang
Jiegou Huaxue (J. Struct. Chem.), 2007
45.
Solvothermal Synthesis, Crystal Structure and DNA Binding Studies of a 3D Supramolecular Complex {[Cu(phen)CN][Cu(phen)][Cu(CN)2]} n Assembled by Double Curvy Chains
Dong F., Li Y., Wu Z., Sun Y., Sun W., Liu Z., Song Y.
Journal of Inorganic and Organometallic Polymers and Materials, 2008
47.
Mechanisms of Tetrazole Formation by Addition of Azide to Nitriles
Himo F., Demko Z.P., Noodleman L., Sharpless K.B.
Journal of the American Chemical Society, 2002
48.
10.1016/j.mencom.2018.11.014_bibe0145
Ostrovskii
2008
49.
Role of cytochrome P 450 IIE1 and catalase in the oxidation of acetonitrile to cyanide
Feierman D.E., Cederbaum A.I.
Chemical Research in Toxicology, 1989
50.
Radical N-cyanation of sulfoximine through acetonitrile CCN cleavage
Hu W., Teng F., Peng H., Yu J., Sun S., Cheng J., Shao Y.
Tetrahedron Letters, 2015
51.
10.1016/j.mencom.2018.11.014_bibe0160
Sheldrick
Acta Crystallogr., 2015
52.
OLEX2: a complete structure solution, refinement and analysis program
Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A., Puschmann H.
Journal of Applied Crystallography, 2009
53.
10.1016/j.mencom.2018.11.014_bibe0170
Spek
Acta Crystallogr., 2015
54.
CrysAlis(Pro), Rigaku Oxford Diffraction, 2017, Version 1.171.39.35a.