Rudolf G Mirskov
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Rudolf G Mirskov has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
- Sergey N. Adamovich
A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Street, 664033 Irkutsk, Russia
4 shared publications A. N. Mirskova
Siberian Branch of the Russian Academy of Sciences
3 shared publicationsM. G. Voronkov
A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russian Federation
2 shared publications- Anna N Mirskova
Siberian Branch of the Russian Academy of Sciences
1 shared publication G. A. Kuznetsova
Siberian Branch of the Russian Academy of Sciences
1 shared publicationI. A. Ushakov
Irkutsk National Research Technical University
1 shared publication
Latest Publications
- 1 March 2016
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 65 (3) , 826-827
New biologically active arylchalcogenylacetates based on triethanolamine N-oxide
- 1 March 2016
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 65 (3) , 826-827
New biologically active arylchalcogenylacetates based on triethanolamine N-oxide
- Open Access
- 19 February 2013
- Published by Springer Nature in BMC Chemistry
- Vol. 7 (1) , 34
Reaction of pharmacological active tris-(2-hydroxyethyl)ammonium 4-chlorophenylsulfanylacetate with ZnCl2 or NiCl2: first conversion of a protic ionic liquid into metallated ionic liquid
The reaction of pharmacological active protic ionic liquid tris-(2-hydroxyethyl)ammonium 4-chlorophenylsulfanylacetate H+N(CH2CH2OH)3 ∙ (-OOCCH2SC6H4Cl-4) (1) with zinc or nickel chloride in a ratio of 2:1 affords stable at room temperature powder-like adducts [H+N(CH2CH2OH)3]2 ∙ [M(OOCCH2SC6H4Cl-4)2Cl2]2-, M = Zn (2), Ni (3). By recrystallization from aqueous alcohol compound 2 unexpectedly gives Zn(OOCCH2SC6H4Cl-4)2 ∙ 2H2O (4). Unlike 2, compound 3 gives crystals [N(CH2CH2OH)3]2Ni2+ · [-OOCCH2SC6H4Cl-4]2 (5), which have a structure of metallated ionic liquid. The structure of 5 has been proved by X-ray diffraction analysis. It is the first example of the conversion of a protic ionic liquid into potentially biological active metallated ionic liquid (1 → 3 → 5).
- 19 February 2013
- Published by Springer Nature in BMC Chemistry
- Vol. 7 (1) , 34
Open AccessReaction of pharmacological active tris-(2-hydroxyethyl)ammonium 4-chlorophenylsulfanylacetate with ZnCl2 or NiCl2: first conversion of a protic ionic liquid into metallated ionic liquid
The reaction of pharmacological active protic ionic liquid tris-(2-hydroxyethyl)ammonium 4-chlorophenylsulfanylacetate H+N(CH2CH2OH)3 ∙ (-OOCCH2SC6H4Cl-4) (1) with zinc or nickel chloride in a ratio of 2:1 affords stable at room temperature powder-like adducts [H+N(CH2CH2OH)3]2 ∙ [M(OOCCH2SC6H4Cl-4)2Cl2]2-, M = Zn (2), Ni (3). By recrystallization from aqueous alcohol compound 2 unexpectedly gives Zn(OOCCH2SC6H4Cl-4)2 ∙ 2H2O (4). Unlike 2, compound 3 gives crystals [N(CH2CH2OH)3]2Ni2+ · [-OOCCH2SC6H4Cl-4]2 (5), which have a structure of metallated ionic liquid. The structure of 5 has been proved by X-ray diffraction analysis. It is the first example of the conversion of a protic ionic liquid into potentially biological active metallated ionic liquid (1 → 3 → 5).
- 1 June 2012
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 61 (6) , 1262-1263
Biologically active aprotic (2-hydroxyethyl)ammonium ionic liquids. Choline derivatives
- 1 June 2012
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 61 (6) , 1262-1263
Biologically active aprotic (2-hydroxyethyl)ammonium ionic liquids. Choline derivatives
- 1 June 2012
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 61 (6) , 1260-1261
Biologically active protic (2-hydroxyethyl)ammonium ionic liquids. Liquid aspirin
- 1 June 2012
- Published by Springer Nature in Russian Chemical Bulletin
- Vol. 61 (6) , 1260-1261
Biologically active protic (2-hydroxyethyl)ammonium ionic liquids. Liquid aspirin