Zobrazeno 1 - 10
of 31
pro vyhledávání: '"I. N. Meshcheryakova"'
Autor:
Alexandr V. Piskunov, Maxim V. Arsenyev, Kseniya V. Arsenyeva, N. M. Khamaletdinova, I. N. Meshcheryakova, Olesya Yu. Trofimova, Irina V. Ershova, Kira I. Pashanova, Ivan V. Smolyaninov, Anton V. Cherkasov
Publikováno v:
Inorganic Chemistry. 60:12309-12322
A series of complexes of metal halides with unreduced quinone-type ligands have been synthesized and characterized in detail. The 3,6-di-tert-butyl-o-benzoquinone (1) and 4,6-di-tert-butyl-N-aryl-substituted o-iminobenzoquinones (2-5) (aryl is 2,6-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e96d4341c3a3750d2eb10716f79fa9a4
https://doi.org/10.1021/acs.inorgchem.1c01514
https://doi.org/10.1021/acs.inorgchem.1c01514
Autor:
Yu. G. Budnikova, Mikhail Khrizanforov, R. R. Aisin, Alexandr V. Piskunov, Nikolay O. Druzhkov, Kira I. Pashanova, Pavel V. Dorovatovskii, O. Yu. Trofimova, I. N. Meshcheryakova, Ilya A. Yakushev
Publikováno v:
Russian Journal of Coordination Chemistry. 47:307-318
Abstract Poorly soluble in the most part of organic solvents dimeric complexes $${\text{M}}{{{\text{g}}}_{{\text{2}}}}{\text{L}}_{2}^{2}$$·4DMF (I) and $${\text{N}}{{{\text{i}}}_{{\text{2}}}}{\text{L}}_{2}^{2}$$·4DMF (II) (L is 4,4'-(1,4-phenyleneb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbcd6db136e6249d63e0d93bebdec882
https://doi.org/10.1134/s1070328421050043
https://doi.org/10.1134/s1070328421050043
Publikováno v:
Journal of Structural Chemistry. 61:1888-1897
We report a comparative analysis of experimental and theoretical vibrational spectra recorded in the frequency region of 700-100 cm–1 for mono-o-iminosemiquinone tin(IV) complexes with general formulas LSnR2Cl (1-5) and LSnR3 (6, 7) (L is the 4,6-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d3e28d0280cc1588e1653b2eaa7f732
https://doi.org/10.1134/s0022476620120069
https://doi.org/10.1134/s0022476620120069
Autor:
I. N. Meshcheryakova, Georgy K. Fukin, Alexandr V. Piskunov, Kseniya V. Arsenyeva, Vladimir K. Cherkasov
Publikováno v:
Mendeleev Communications. 30:592-595
N-Heterocyclic carbene is a versatile ligand for the preparation of copper( i ) and silver( i ) derivatives bearing the radical anion forms of redox active o-benzoquinone and o-iminobenzoquinone. The paramagnetic three-coordinated copper( i ) and sil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a7f8052f2697f32c6ab17d658a6583a
https://doi.org/10.1016/j.mencom.2020.09.013
https://doi.org/10.1016/j.mencom.2020.09.013
Autor:
I. N. Meshcheryakova, Alexandr V. Piskunov, A. S. Bogomyakov, Georgy K. Fukin, E. V. Baranov, Alexey A. Zolotukhin, M. P. Bubnov, N. A. Skorodumova, Vladimir K. Cherkasov
Publikováno v:
Russian Journal of Coordination Chemistry. 46:224-240
Metal tris-o-dioxolene (o-quinone, o-semiquinone, and catecholate) complexes represent an interesting and vivid model system for the demonstration of a relationship between the structure and magnetic properties when considering a series of objects of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f62616a9e0b8621d3a9fc96a41aa2d16
https://doi.org/10.1134/s107032842003001x
https://doi.org/10.1134/s107032842003001x
Publikováno v:
Russian Chemical Bulletin. 69:49-60
New bis-p-iminobenzoquinone ligands, in which two hydroxy-p-iminobenzoquinone moieties are bridged by various functionalized linkers, were synthesized by 1,4-addition of aromatic diamines to 3,6-di-tert-butyl-o-benzoquinone. The exchange reaction bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::424c93eea20f055de19f684263f5c291
https://doi.org/10.1007/s11172-020-2722-x
https://doi.org/10.1007/s11172-020-2722-x
Autor:
I. N. Meshcheryakova, Olesya Yu. Trofimova, Rinat R. Aysin, Alexandr D. Kharitonov, Yulia H. Budnikova, Konstantin A. Kovalenko, Mikhail Khrizanforov, Alexandr V. Piskunov, Georgy K. Fukin, Artem S. Bogomyakov
Publikováno v:
CrystEngComm. 22:4675-4679
The synthesis, crystal structure, thermal stability, porosity and magnetic properties of three new layered coordination polymers [(M2(pQ)3)·4DMAA]n (M3+ = La3+ (1), Pr3+ (2), Nd3+ (3); pQ2− – the dianionic form of 2,5-dihydroxy-3,6-di-tert-butyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3654534c56f5b72265a2b4c8ca8dca1d
https://doi.org/10.1039/d0ce00767f
https://doi.org/10.1039/d0ce00767f
Autor:
I. N. Meshcheryakova, Stanislav P. Kubrin, Nikolay V. Somov, Artyem S. Bogomyakov, Marina S. Piskunova, Alexandr V. Piskunov
Publikováno v:
Journal of Molecular Structure. 1195:417-425
By the metal salt metathesis reaction between tin(IV) bis-o-iminobenzosemiquinonates imSQi−Pr2SnCl2 (1) or imSQMe2SnCl2 (2) (where imSQi-Pr – radical-anion of N-2,6-di-iso-propylphenylsubstituted o-iminobenzoquinone, imSQMe - radical-anion of N-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d49f37bd91176365c2c0f19752b87230
https://doi.org/10.1016/j.molstruc.2019.05.126
https://doi.org/10.1016/j.molstruc.2019.05.126
Publikováno v:
Russian Chemical Bulletin. 68:1414-1423
Two synthetic approaches were used for the synthesis of 3,6-di-tert-butylcatecholate derivatives of titanium(iv). These approaches are based on the exchange reaction between sodium catecholate and titanium(iv) chloride and the reaction of 3,6-di-tert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf2f9e17fff7287ceb1fa16d19fd83b1
https://doi.org/10.1007/s11172-019-2570-8
https://doi.org/10.1007/s11172-019-2570-8
Autor:
Nikolay O. Druzhkov, Ivan V. Smolyaninov, I. N. Meshcheryakova, Georgy K. Fukin, A. I. Poddel’skii, L. S. Okhlopkova
Publikováno v:
Russian Journal of Coordination Chemistry. 45:133-141
New catecholate complexes of triphenylantimony(V), (Etgly-3,6-DBCat)SbPh3 (I), (Propgly-3,6-DBCat)SbPh3 (II), and (Cat-3,6-DBCat)SbPh3 (III), based on analogs of sterically hindered 3,6-di-tert-butyl-o-benzoquinone, 5,8-di-tert-butyl-2,3-dihydrobenzo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::772d1fa3cbbe7c6e6ac7a33a433de082
https://doi.org/10.1134/s1070328419010093
https://doi.org/10.1134/s1070328419010093