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Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles

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Chulanova E. A. et al. Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles // Mendeleev Communications. 2018. Vol. 28. No. 5. pp. 453-460.
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Chulanova E. A., Semenov N. A., Pushkarevsky N. A., Gritsan N. P., Zibarev A. V. Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles // Mendeleev Communications. 2018. Vol. 28. No. 5. pp. 453-460.
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TY - JOUR
DO - 10.1016/j.mencom.2018.09.001
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.09.001
TI - Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles
T2 - Mendeleev Communications
AU - Chulanova, Elena Aleksandrovna
AU - Semenov, Nikolay Andreevich
AU - Pushkarevsky, Nikolay Anatol'evich
AU - Gritsan, Nina Pavlovna
AU - Zibarev, Andrey Viktorovich
PY - 2018
DA - 2018/09/07
PB - Mendeleev Communications
SP - 453-460
IS - 5
VL - 28
ER -
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@article{2018_Chulanova,
author = {Elena Aleksandrovna Chulanova and Nikolay Andreevich Semenov and Nikolay Anatol'evich Pushkarevsky and Nina Pavlovna Gritsan and Andrey Viktorovich Zibarev},
title = {Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles},
journal = {Mendeleev Communications},
year = {2018},
volume = {28},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.09.001},
number = {5},
pages = {453--460},
doi = {10.1016/j.mencom.2018.09.001}
}
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Chulanova, Elena Aleksandrovna, et al. “Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles.” Mendeleev Communications, vol. 28, no. 5, Sep. 2018, pp. 453-460. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.09.001.
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Abstract

Recent achievements in the charge-transfer chemistry of 1,2,5-chalcogenadiazoles, 1,2,3-dichalcogenazoles (chalcogen is S, Se, or Te), their fused congeners and hybrids are discussed with special emphasis on the synthesis and structural and functional characterization of radical anions, radical-anion salts, charge-transfer complexes, neutral and charged donor–acceptor complexes, and metal coordination compounds.

References

1.
10.1016/j.mencom.2018.09.001_sbref0005a
Chivers
A Guide to Chalcogen–Nitrogen Chemistry, 2005
2.
10.1016/j.mencom.2018.09.001_sbref0005b
Zibarev
Selenium and Tellurium Chemistry: From Small Molecules to Biomolecules and Materials, 2011
3.
Benzothiadiazole Derivatives as Fluorescence Imaging Probes: Beyond Classical Scaffolds
Neto B.A., Carvalho P.H., Correa J.R.
Accounts of Chemical Research, 2015
4.
Molecular Dynamics Simulation of the Solid-State Topochemical Polymerization of S2N2
Takaluoma T.T., Laasonen K., Laitinen R.S.
Inorganic Chemistry, 2013
6.
Polysulfur nitride - a metallic, superconducting polymer
Labes M.M., Love P., Nichols L.F.
Chemical Reviews, 1979
7.
Spin Frustration in an Organic Radical Ion Salt Based on a Kagome-Coupled Chain Structure
Postulka L., Winter S.M., Mihailov A.G., Mailman A., Assoud A., Robertson C.M., Wolf B., Lang M., Oakley R.T.
Journal of the American Chemical Society, 2016
8.
Magnetic Ordering and Anisotropy in Heavy Atom Radicals
Winter S.M., Hill S., Oakley R.T.
Journal of the American Chemical Society, 2015
9.
Supramolecular architecture, crystal structure and transport properties of the prototypal oxobenzene-bridged bisdithiazolyl radical conductor
Wong J.W., Mailman A., Winter S.M., Robertson C.M., Holmberg R.J., Murugesu M., Dube P.A., Oakley R.T.
Chemical Communications, 2014
11.
Hybrid dithiazolothiadiazinyl radicals; versatile building blocks for magnetic and conductive materials
Winter S.M., Balo A.R., Roberts R.J., Lekin K., Assoud A., Dube P.A., Oakley R.T.
Chemical Communications, 2013
12.
Spin-orbit effects in heavy-atom organic radical ferromagnets
Winter S.M., Oakley R.T., Kovalev A.E., Hill S.
Physical Review B, 2012
14.
10.1016/j.mencom.2018.09.001_sbref0015h
Stable Radicals: Fundamentals and Applied Aspects of Odd Electron Compounds, 2010
15.
10.1016/j.mencom.2018.09.001_sbref0015i
Rawson
Handbook of Chalcogen Chemistry: New Perspectives in Sulfur, Selenium and Tellurium, 2007
16.
Spin, charge and lattice correlation in thiazyl radicals and their molecular compounds
Awaga K., Tanaka T., Shirai T., Umezono Y., Fujita W.
Comptes Rendus Chimie, 2007
19.
A novel sulfur–nitrogen π-heterocyclic radical anion, (6H-1,2,3-benzodithiazol-6-ylidene)malononitrilidyl, and its homo- and heterospin salts
Makarov A.Y., Chulanova E.A., Semenov N.A., Pushkarevsky N.A., Lonchakov A.V., Bogomyakov A.S., Irtegova I.G., Vasilieva N.V., Lork E., Gritsan N.P., Konchenko S.N., Ovcharenko V.I., Zibarev A.V.
Polyhedron, 2014
20.
Chulanova E.A., Irtegova I.G., Vasilieva N.V., Bagryanskaya I.Y., Gritsan N.P., Zibarev A.V.
Mendeleev Communications, 2015
21.
Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange
Konstantinova L.S., Baranovsky I.V., Pritchina E.A., Mikhailov M.S., Bagryanskaya I.Y., Semenov N.A., Irtegova I.G., Salnikov G.E., Lyssenko K.A., Gritsan N.P., Zibarev A.V., Rakitin O.A.
Chemistry - A European Journal, 2017
22.
New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction
Chulanova E.A., Pritchina E.A., Malaspina L.A., Grabowsky S., Mostaghimi F., Beckmann J., Bagryanskaya I.Y., Shakhova M.V., Konstantinova L.S., Rakitin O.A., Gritsan N.P., Zibarev A.V.
Chemistry - A European Journal, 2016
23.
Donor-Acceptor Complexes between 1,2,5-Chalcogenadiazoles (Te, Se, S) and the Pseudohalides CN− and XCN− (X=O, S, Se, Te)
Semenov N.A., Gorbunov D.E., Shakhova M.V., Salnikov G.E., Bagryanskaya I.Y., Korolev V.V., Beckmann J., Gritsan N.P., Zibarev A.V.
Chemistry - A European Journal, 2018
24.
10.1016/j.mencom.2018.09.001_sbref0020g
Pushkarevsky
Chem. Eur. J., 2018
25.
Inter-molecule interaction for magnetic property of vanadyl tetrakis(thiadiazole) porphyrazine film on Au(1 1 1)
Hou J., Wang Y., Eguchi K., Nanjo C., Takaoka T., Sainoo Y., Awaga K., Komeda T.
Applied Surface Science, 2018
26.
Perfluorinated subphthalocynine analogues containing fused 1,2,5-thiadiazole fragments
Hamdoush M., Skvortsov I.A., Mikhailov M.S., Pakhomov G., Stuzhin P.A.
Journal of Fluorine Chemistry, 2017
27.
DFT Study of molecular and electronic structure of magnesium (II) tetra(1,2,5-chalcogenadiazolo) porphyrazines, [TXDPzMg] (X = O, S, Se, Te)
Zhabanov Y.A., Tverdova N.V., Giricheva N.I., Girichev G.V., Stuzhin P.A.
Journal of Porphyrins and Phthalocyanines, 2017
29.
1,2,5-chalcogenadiazole-annulated tripyrazinoporphyrazines: Synthesis, spectral characteristics, and influence of the heavy atom effect on their photophysical properties
Svec J., Zimcik P., Novakova L., Rakitin O.A., Amelichev S.A., Stuzhin P.A., Novakova V.
European Journal of Organic Chemistry, 2014
30.
First tellurium-containing phthalocyanine analogues: Strong effect of tellurium on spectral, redox and conductivity properties of porphyrazines with annulated chalcogenodiazole ring(s)
Stuzhin P.A., Mikhailov M.S., Yurina E.S., Bazanov M.I., Koifman O.I., Pakhomov G.L., Travkin V.V., Sinelshchikova A.A.
Chemical Communications, 2012
31.
Crystal Structure, Spin Polarization, Solid-State Electrochemistry, and High n-Type Carrier Mobility of a Paramagnetic Semiconductor: Vanadyl Tetrakis(thiadiazole)porphyrazine
Miyoshi Y., Takahashi K., Fujimoto T., Yoshikawa H., Matsushita M.M., Ouchi Y., Kepenekian M., Robert V., Donzello M.P., Ercolani C., Awaga K.
Inorganic Chemistry, 2011
33.
Salts of Sterically Hindered Chalcogen-Varied Herz Cations Including Those with [Te3 Cl14 ]2- and [Te4 Cl18 ]2- Anions
Makarov A.Y., Bagryanskaya I.Y., Volkova Y.M., Shakirov M.M., Zibarev A.V.
European Journal of Inorganic Chemistry, 2018
34.
Volkova Y.M., Makarov A.Y., Zikirin S.B., Genaev A.M., Bagryanskaya I.Y., Zibarev A.V.
Mendeleev Communications, 2017
35.
Stable N- and N/S-Rich Heterocyclic Radicals
Constantinides C.P., Koutentis P.A.
Advances in Heterocyclic Chemistry, 2016
36.
A 1,2,3-dithiazolyl-o-naphthoquinone: a neutral radical with isolable cation and anion oxidation states
Smithson C.S., MacDonald D.J., Matt Letvenuk T., Carello C.E., Jennings M., Lough A.J., Britten J., Decken A., Preuss K.E.
Dalton Transactions, 2016
38.
Stable heterocyclic radicals
Rakitin O.A.
Russian Chemical Reviews, 2011
39.
Pulse EPR and ENDOR study of 1,2,3-benzodithiazolyl, 2,1,3-benzothiaselenazolyl and 1,2,3-benzodiselenazolyl radicals
Pivtsov A.V., Kulik L.V., Makarov A.Y., Blockhuys F.
Physical Chemistry Chemical Physics, 2011
40.
A New Approach to Chalcogen–Nitrogen π-Heterocyclic Radicals
Gritsan N.P., Makarov A.Y., Zibarev A.V.
Applied Magnetic Resonance, 2011
41.
Thiazyl radicals: old materials for new molecular devices
Rawson J.M., Alberola A., Whalley A.
Journal of Materials Chemistry A, 2006
43.
Reaction of Herz salts with malononitrile: a general route to (6H-1,2,3-benzodithiazol-6-ylidene)malononitriles
Koutentis P.A., Rees C.W.
Journal of the Chemical Society Perkin Transactions 1, 2002
44.
10.1016/j.mencom.2018.09.001_bib0045
IUPAC Compendium of Chemical Terminology (The Gold Book), 1997
45.
Fused 1,2,3-dithiazoles: Convenient synthesis, structural characterization, and electrochemical properties
Konstantinova L., Baranovsky I., Irtegova I., Bagryanskaya I., Shundrin L., Zibarev A., Rakitin O.
Molecules, 2016
46.
Recent Developments in the Synthesis and Applications of 1,2,5-Thia-and Selenadiazoles. A Review
Konstantinova L.S., Knyazeva E.A., Rakitin O.A.
Organic Preparations and Procedures International, 2014
47.
2,1,3-Benzothiadiazole and Derivatives: Synthesis, Properties, Reactions, and Applications in Light Technology of Small Molecules
Neto B.A., Lapis A.A., da Silva Júnior E.N., Dupont J.
European Journal of Organic Chemistry, 2012
48.
10.1016/j.mencom.2018.09.001_sbref0050d
Todres
Chalcogenadiazoles: Chemistry and Applications, 2012
49.
A survey of tellurium-centered secondary-bonding supramolecular synthons
Cozzolino A.F., Elder P.J., Vargas-Baca I.
Coordination Chemistry Reviews, 2011
50.
10.1016/j.mencom.2018.09.001_sbref0050f
Koutentis
2008
51.
10.1016/j.mencom.2018.09.001_sbref0050g
Rakitin
2008
52.
Synthesis and properties of 1,2,3-dithiazoles
Konstantinova L.S., Rakitin O.A.
Russian Chemical Reviews, 2008
53.
Shundrin L.A., Irtegova I.G., Avrorov P.A., Mikhailovskaya T.F., Makarov A.G., Makarov A.Y., Zibarev A.V.
Arkivoc, 2017
54.
Selenadiazolo[3,4-b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selenadiazole and Generation of Persistent Radical Anions
Konstantinova L.S., Bobkova I.E., Nelyubina Y.V., Chulanova E.A., Irtegova I.G., Vasilieva N.V., Camacho P.S., Ashbrook S.E., Hua G., Slawin A.M., Woollins J.D., Zibarev A.V., Rakitin O.A.
European Journal of Organic Chemistry, 2015
55.
Redox properties and radical anions of fluorinated 2,1,3-benzothia(selena)diazoles and related compounds
Vasilieva N.V., Irtegova I.G., Gritsan N.P., Lonchakov A.V., Makarov A.Y., Shundrin L.A., Zibarev A.V.
Journal of Physical Organic Chemistry, 2010
56.
Konstantinova L.S., Bol'shakov O.I., Baranovsky I.V., Bogacheva A.M., Strunyasheva V.V., Rakitin O.A.
Mendeleev Communications, 2015
59.
Reactions of vicinal nitroamines with sulfur monochloride - A short and convenient route to fused 1,2,5-thiadiazoles and their N-oxides
Konstantinova L.S., Knyazeva E.A., Obruchnikova N.V., Gatilov Y.V., Zibarev A.V., Rakitin O.A.
Tetrahedron Letters, 2013
62.
Dye-sensitized solar cells: Investigation of D-A-Π-A organic sensitizers based on [1,2,5]selenadiazolo[3,4-c]pyridine
Knyazeva E.A., Wu W., Chmovzh T.N., Robertson N., Woollins J.D., Rakitin O.A.
Solar Energy, 2017
64.
Novel applications of functionalized 2,1,3-benzothiadiazoles for coordination chemistry and crystal engineering
Bashirov D.A., Sukhikh T.S., Kuratieva N.V., Chulanova E.A., Yushina I.V., Gritsan N.P., Konchenko S.N., Zibarev A.V.
RSC Advances, 2014
65.
First charge-transfer complexes between tetrathiafulvalene and 1,2,5-chalcogenadiazole derivatives: Design, synthesis, crystal structures, electronic and electrical properties
Pushkarevsky N.A., Lonchakov A.V., Semenov N.A., Lork E., Buravov L.I., Konstantinova L.S., Silber G.T., Robertson N., Gritsan N.P., Rakitin O.A., Woollins J.D., Yagubskii E.B., Beckmann J., Zibarev A.V.
Synthetic Metals, 2012
67.
The Nature of the Supramolecular Association of 1,2,5-Chalcogenadiazoles
Cozzolino A.F., Vargas-Baca I., Mansour S., Mahmoudkhani A.H.
Journal of the American Chemical Society, 2005
69.
The role of the Lewis acid−base properties in the supramolecular association of 1,2,5-chalcogenadiazoles
Cozzolino A.F., Elder P.J., Lee L.M., Vargas-Baca I.
Canadian Journal of Chemistry, 2013
70.
Supramolecular Synthesis Based on a Combination of Se···N Secondary Bonding Interactions with Hydrogen and Halogen Bonds
Eichstaedt K., Wasilewska A., Wicher B., Gdaniec M., Połoński T.
Crystal Growth and Design, 2016
71.
The size of the metal ion controls the structures of the coordination polymers of benzo-2,1,3-selenadiazole
Lee L.M., Elder P.J., Dube P.A., Greedan J.E., Jenkins H.A., Britten J.F., Vargas-Baca I.
CrystEngComm, 2013
72.
Iridium complexes with 2,1,3-benzothiadiazole and related ligands
Bashirov D.A., Sukhikh T.S., Kuratieva N.V., Naumov D.Y., Konchenko S.N., Semenov N.A., Zibarev A.V.
Polyhedron, 2012
73.
Crystal engineering with 2,1,3-benzoselenadiazole and mercury(II) chloride
Milios C.J., Ioannou P.V., Raptopoulou C.P., Papaefstathiou G.S.
Polyhedron, 2009
74.
New molecular complexes of trimeric perfluoro-ortho-phenylene mercury with heterocyclic compounds
Semenov N.A., Bagryanskaya I.Y., Alekseev A.V., Gatilov Y.V., Lork E., Mews R., Roeschentaler G.-., Zibarev A.V.
Journal of Structural Chemistry, 2010
76.
Trimeric Perfluoro-ortho-phenylenemercury: A Versatile Lewis Acidic Host
Haneline M.R., Taylor R.E., Gabbaï F.P.
Chemistry - A European Journal, 2003
79.
Frustrated Lewis pairs: from concept to catalysis.
Stephan D.W.
Accounts of Chemical Research, 2014
80.
Frustrated Lewis Pair Chemistry: Development and Perspectives
Stephan D.W., Erker G.
Angewandte Chemie - International Edition, 2015
81.
“Frustrated Lewis pairs”: a concept for new reactivity and catalysis
82.
3D molecular network and magnetic ordering, formed by multi-dentate magnetic couplers, bis(benzene)chromium(i) and [1,2,5]thiadiazolo[3,4-: C] [1,2,5]thiadiazolidyl
Shuku Y., Hirai Y., Semenov N.A., Kadilenko E., Gritsan N.P., Zibarev A.V., Rakitin O.A., Awaga K.
Dalton Transactions, 2018
83.
Synthesis and Properties of the Heterospin (S1 = S2 = 1/2) Radical-Ion Salt Bis(mesitylene)molybdenum(I) [1,2,5]Thiadiazolo[3,4- c ][1,2,5]thiadiazolidyl
Pushkarevsky N.A., Semenov N.A., Dmitriev A.A., Kuratieva N.V., Bogomyakov A.S., Irtegova I.G., Vasilieva N.V., Bode B.E., Gritsan N.P., Konstantinova L.S., Woollins J.D., Rakitin O.A., Konchenko S.N., Ovcharenko V.I., Zibarev A.V., et. al.
Inorganic Chemistry, 2015
84.
Bis(toluene)chromium(I) [1,2,5]Thiadiazolo[3,4-c ][1,2,5]thiadiazolidyl and [1,2,5]Thiadiazolo[3,4-b ]pyrazinidyl: New heterospin (S 1 = S 2 = 1/2) radical-ion salts
Semenov N.A., Pushkarevsky N.A., Suturina E.A., Chulanova E.A., Kuratieva N.V., Bogomyakov A.S., Irtegova I.G., Vasilieva N.V., Konstantinova L.S., Gritsan N.P., Rakitin O.A., Ovcharenko V.I., Konchenko S.N., Zibarev A.V.
Inorganic Chemistry, 2013
85.
Heterospin π-Heterocyclic Radical-Anion Salt: Synthesis, Structure, and Magnetic Properties of Decamethylchromocenium [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl
Semenov N.A., Pushkarevsky N.A., Lonchakov A.V., Bogomyakov A.S., Pritchina E.A., Suturina E.A., Gritsan N.P., Konchenko S.N., Mews R., Ovcharenko V.I., Zibarev A.V.
Inorganic Chemistry, 2010
86.
Konchenko S.N., Gritsan N.P., Lonchakov A.V., Radius U., Zibarev A.V.
Mendeleev Communications, 2009
87.
Cobaltocenium [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl: Synthesis, Structure, and Magnetic Properties
Konchenko S.N., Gritsan N.P., Lonchakov A.V., Irtegova I.G., Mews R., Ovcharenko V.I., Radius U., Zibarev A.V.
European Journal of Inorganic Chemistry, 2008
89.
[1,2,5]Selenadiazolo[3,4-c][1,2,5]thiadiazole and [1,2,5]Selenadiazolo[3,4-c][1,2,5]thiadiazolidyl – A Synthetic, Structural, and Theoretical Study
Bagryanskaya I.Y., Gatilov Y.V., Gritsan N.P., Ikorskii V.N., Irtegova I.G., Lonchakov A.V., Lork E., Mews R., Ovcharenko V.I., Semenov N.A., Vasilieva N.V., Zibarev A.V.
European Journal of Inorganic Chemistry, 2007
90.
Early Alkali Metal (Li, Na, K) and Tris(dimethylamino)sulfonium (TAS) Salts of [1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl Radical Anion: Rational Syntheses, Structures and Magnetic Properties
91.
[1,2,5]Thiadiazolo[3,4-c][1,2,5]thiadiazolidyl:  A Long-Lived Radical Anion and Its Stable Salts
Makarov A.Y., Irtegova I.G., Vasilieva N.V., Bagryanskaya I.Y., Borrmann T., Gatilov Y.V., Lork E., Mews R., Stohrer W., Zibarev A.V.
Inorganic Chemistry, 2005
92.
E.A. Radiush, Diploma Thesis, Novosibirsk State University, Novosibirsk, 2018.
93.
10.1016/j.mencom.2018.09.001_sbref0110b
Radiush
4th European Crystallography School (ECS4), 2017
95.
Spin-orbit coupling in molecules: Chemistry beyond the adiabatic approximation
Fedorov D.G., Koseki S., Schmidt M.W., Gordon M.S.
International Reviews in Physical Chemistry, 2003
96.
10.1016/j.mencom.2018.09.001_sbref0120b
Marian
2001
97.
10.1016/j.mencom.2018.09.001_sbref0120c
Kahn
Molecular Magnetism, 1993
98.
McConnell I mechanism promotes ferromagnetic interactions between π-stacked Ni(ii)–thiazyl complexes
Fatila E.M., Clérac R., Jennings M., Preuss K.E.
Chemical Communications, 2013
101.
[TDNQ][CoCp*2] and [TDNQ]3[CoCp2]2; Radical Anions of a 1,2,5-Thiadiazolo-naphthoquinone
Morgan I.S., Jennings M., Vindigni A., Clérac R., Preuss K.E.
Crystal Growth and Design, 2011
103.
The First Lanthanide Complexes with a Redox-Active Sulfur Diimide Ligand: Synthesis and Characterization of [LnCp*2(RN=)2S], Ln=Sm, Eu, Yb; R=SiMe3
Klementyeva S.V., Gritsan N.P., Khusniyarov M.M., Witt A., Dmitriev A.A., Suturina E.A., Hill N.D., Roemmele T.L., Gamer M.T., Boeré R.T., Roesky P.W., Zibarev A.V., Konchenko S.N.
Chemistry - A European Journal, 2016
104.
Hirshfeld surface analysis
Spackman M.A., Jayatilaka D.
CrystEngComm, 2009
105.
Novel tools for visualizing and exploring intermolecular interactions in molecular crystals
McKinnon J.J., Spackman M.A., Mitchell A.S.
Acta Crystallographica Section B Structural Science, 2004
106.
Nature of Bonding in Donor-Acceptor Interactions Exemplified by Complexes of N-Heterocyclic Carbenes with 1,2,5-Telluradiazoles
Pushkarevsky N.A., Petrov P.A., Grigoriev D.S., Smolentsev A.I., Lee L.M., Kleemiss F., Salnikov G.E., Konchenko S.N., Vargas-Baca I., Grabowsky S., Beckmann J., Zibarev A.V.
Chemistry - A European Journal, 2017
107.
Donor-acceptor coordination of anions by chalcogen atoms of 1,2,5-chalcogenadiazoles
Semenov N.A., Lonchakov A.V., Gritsan N.P., Zibarev A.V.
Russian Chemical Bulletin, 2015
108.
Coordination of Halide and Chalcogenolate Anions to Heavier 1,2,5-Chalcogenadiazoles: Experiment and Theory
Semenov N.A., Lonchakov A.V., Pushkarevsky N.A., Suturina E.A., Korolev V.V., Lork E., Vasiliev V.G., Konchenko S.N., Beckmann J., Gritsan N.P., Zibarev A.V.
Organometallics, 2014
109.
Tellurium-Nitrogen π-Heterocyclic Chemistry - Synthesis, Structure, and Reactivity Toward Halides and Pyridine of 3,4-Dicyano-1,2,5-telluradiazole
Semenov N.A., Pushkarevsky N.A., Beckmann J., Finke P., Lork E., Mews R., Bagryanskaya I.Y., Gatilov Y.V., Konchenko S.N., Vasiliev V.G., Zibarev A.V.
European Journal of Inorganic Chemistry, 2012
110.
Interaction of 1,2,5-Chalcogenadiazole Derivatives with Thiophenolate: Hypercoordination with Formation of Interchalcogen Bond versus Reduction to Radical Anion
Suturina E.A., Semenov N.A., Lonchakov A.V., Bagryanskaya I.Y., Gatilov Y.V., Irtegova I.G., Vasilieva N.V., Lork E., Mews R., Gritsan N.P., Zibarev A.V.
Journal of Physical Chemistry A, 2011
111.
Characterization of chalcogen bonding interactions via an in-depth conceptual quantum chemical analysis
De Vleeschouwer F., Denayer M., Pinter B., Geerlings P., De Proft F.
Journal of Computational Chemistry, 2017
112.
Chalcogen Bonding in Solution: Interactions of Benzotelluradiazoles with Anionic and Uncharged Lewis Bases
Garrett G.E., Gibson G.L., Straus R.N., Seferos D.S., Taylor M.S.
Journal of the American Chemical Society, 2015
114.
Anion Recognition Strategies Based on Combined Noncovalent Interactions
115.
Anion Receptor Chemistry
Gale P., Howe E.W., Wu X.
Chem, 2016
116.
Anion receptor chemistry: highlights from 2011 and 2012
Gale P.A., Busschaert N., Haynes C.J., Karagiannidis L.E., Kirby I.L.
Chemical Society Reviews, 2014
117.
Benzoselenadiazole Fluorescent Probes – Near-IR Optical and Ratiometric Fluorescence Sensor for Fluoride Ion
Saravanan C., Easwaramoorthi S., Hsiow C., Wang K., Hayashi M., Wang L.
Organic Letters, 2013
118.
Anion receptor chemistry.
Gale P.A.
Chemical Communications, 2011
119.
Fluorogenic and Chromogenic Chemosensors and Reagents for Anions
Martínez-Máñez R., Sancenón F.
Chemical Reviews, 2003
121.
Novel luminescent β-ketoimine derivative of 2,1,3-benzothiadiazole: synthesis, complexation with Zn(ii) and photophysical properties in comparison with related compounds
Sukhikh T.S., Bashirov D.A., Ogienko D.S., Kuratieva N.V., Sherin P.S., Rakhmanova M.I., Chulanova E.A., Gritsan N.P., Konchenko S.N., Zibarev A.V.
RSC Advances, 2016
122.
New NIR-emissive tetranuclear Er(iii) complexes with 4-hydroxo-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands: synthesis and characterization
Sukhikh T.S., Bashirov D.A., Kuratieva N.V., Smolentsev A.I., Bogomyakov A.S., Burilov V.A., Mustafina A.R., Zibarev A.V., Konchenko S.N.
Dalton Transactions, 2015
123.
New red-luminescent cadmium coordination polymers with 4-amino-2,1,3-benzothiadiazole
Sukhikh T.S., Ogienko D.S., Bashirov D.A., Kuratieva N.V., Komarov V.Y., Rakhmanova M.I., Konchenko S.N.
Journal of Coordination Chemistry, 2016
124.
Synthesis, luminescent and magnetic properties of new tetranuclear lanthanide complexes with 4-hydroxy-2,1,3-benzothiadiazolate and dibenzoylmethanide ligands
Sukhikh T.S., Bashirov D.A., Kolybalov D.S., Andreeva A.Y., Smolentsev A.I., Kuratieva N.V., Burilov V.A., Mustafina A.R., Kozlova S.G., Konchenko S.N.
Polyhedron, 2017
125.
The hows and whys of peculiar coordination of 4-amino-2,1,3-benzothiadiazole
Sukhikh T.S., Komarov V.Y., Konchenko S.N., Benassi E.
Polyhedron, 2018
126.
Noncovalent interactions and photophysical properties of new Ag(I) complexes with 4-amino-2,1,3-benzothiadiazole
Sukhikh T.S., Bashirov D.A., Shuvaev S., Komarov V.Y., Kuratieva N.V., Konchenko S.N., Benassi E.
Polyhedron, 2018
127.
Trinuclear Mn(ii) complex with paramagnetic bridging 1,2,3-dithiazolyl ligands
Sullivan D.J., Clérac R., Jennings M., Lough A.J., Preuss K.E.
Chemical Communications, 2012
129.
Anion recognition by a bidentate chalcogen bond donor
Garrett G.E., Carrera E.I., Seferos D.S., Taylor M.S.
Chemical Communications, 2016
131.
Topological reaction sites – very strong chalcogen bonds
Alikhani E., Fuster F., Madebene B., Grabowski S.J.
Physical Chemistry Chemical Physics, 2014
133.
The Halogen Bond
Cavallo G., Metrangolo P., Milani R., Pilati T., Priimagi A., Resnati G., Terraneo G.
Chemical Reviews, 2016
134.
10.1016/j.mencom.2018.09.001_sbref0185a
Gamez
Chem. Commun., 2011
135.
Organoselenium Chemistry: Role of Intramolecular Interactions
Mukherjee A.J., Zade S.S., Singh H.B., Sunoj R.B.
Chemical Reviews, 2010
136.
10.1016/j.mencom.2018.09.001_sbref0185c
Handbook of Chalcogen Chemistry. New Perspectives in Sulfur, Selenium and Tellurium, 2007
137.
Quantification of Intramolecular Nonbonding Interactions in Organochalcogens
138.
Theoretical Investigations on Chalcogen−Chalcogen Interactions:  What Makes These Nonbonded Interactions Bonding?
Bleiholder C., Werz D.B., Köppel H., Gleiter R.
Journal of the American Chemical Society, 2006
139.
Intramolecular Nonbonding Interactions between Selenium and Sulfur – Spectroscopic Evidence and Importance in Asymmetric Synthesis
Tiecco M., Testaferri L., Santi C., Tomassini C., Santoro S., Marini F., Bagnoli L., Temperini A., Costantino F.
European Journal of Organic Chemistry, 2006
140.
Nucleophilic Attack at Selenium in Diselenides and Selenosulfides. A Computational Study
Bachrach S.M., Demoin D.W., Luk M., Miller J.V.
Journal of Physical Chemistry A, 2004
141.
Asymmetric Azidoselenenylation of Alkenes: A Key Step for the Synthesis of Enantiomerically Enriched Nitrogen‐Containing Compounds
Tiecco M., Testaferri L., Santi C., Tomassini C., Marini F., Bagnoli L., Temperini A.
Angewandte Chemie, 2003
142.
Preparation of a New Chiral Non-Racemic Sulfur-Containing Diselenide and Applications in Asymmetric Synthesis
Tiecco M., Testaferri L., Santi C., Tomassini C., Marini F., Bagnoli L., Temperini A.
Chemistry - A European Journal, 2002
143.
1,2,5-Thiadiazole 2-oxides: Selective synthesis, structural characterization, and electrochemical properties
Konstantinova L.S., Knyazeva E.A., Obruchnikova N.V., Vasilieva N.V., Irtegova I.G., Nelyubina Y.V., Bagryanskaya I.Y., Shundrin L.A., Sosnovskaya Z.Y., Zibarev A.V., Rakitin O.A.
Tetrahedron, 2014
144.
Nitro derivatives of 2,1,3-benzothiadiazole 1-oxides: synthesis, structural study, and NO release
Konstantinova L.S., Knyazeva E.A., Gatilov Y.V., Zlotin S.G., Rakitin O.A.
Russian Chemical Bulletin, 2018
145.
New Polysulfur-Nitrogen Heterocycles by Thermolysis of 1,3λ4δ2,2,4-Benzodithiadiazines in the Hydrocarbon and Fluorocarbon Series
Zhivonitko V.V., Makarov A.Y., Bagryanskaya I.Y., Gatilov Y.V., Shakirov M.M., Zibarev A.V.
European Journal of Inorganic Chemistry, 2005
146.
10.1016/j.mencom.2018.09.001_bib0200
Smart Materials, 2008
147.
N. D. D. Hill, R. T. Boere, 99th Canadian Chemistry Conference and Exhibition, 2016, Abstract 00809.
148.
Experimental and Theoretical Studies of Unusual Four‐Membered Metallacycles from Reactions of Group 4 Metallocene Bis(trimethylsilyl)acetylene Complexes with the Sulfurdiimide Me 3 SiN=S=NSiMe 3
Kaleta K., Ruhmann M., Theilmann O., Roy S., Beweries T., Arndt P., Villinger A., Jemmis E.D., Schulz A., Rosenthal U.
European Journal of Inorganic Chemistry, 2011
149.
Skeletal scrambling of sulphur diimide radical anions
Bestari K., Oakley R.T., Cordes A.W.
Canadian Journal of Chemistry, 1991
152.
Polyimido sulfur anions and ylides
Stalke D.
Chemical Communications, 2012
153.
Preparation and Structure of [Li2Se(NtBu)3]2, Containing the Novel Se(NtBu)32- Anion
155.
Schwefel‐Anionen mit der Koordinationszahl 3: Synthese, Struktur und Existenzbereich
Roesky H.W., Schmieder W., Isenberg W., Sheldrick W.S., Sheldrick G.M.
Chemische Berichte, 1982