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1.
Mikhailov Oleg V. Kazymova Marina A. Shumilova Tatyana A. Solovieva Svetlana S. 《Transition Metal Chemistry》2003,28(6):665-667
The complexing processes in the triple copper(II)–thiocarbohydrazide–propanone system taking place in a copper(II) hexacyanoferrate(II) gelatin-immobilized matrix in contact with aqueous-alkaline solutions (pH12), containing thiocarbohydrazide and propanone, have been studied. Template synthesis leading to a macrocyclic coordination compound with the tetradentate N,N,S,S-donor ligand, (4,4,6-trimethyl-2,3,7,8-tetraazanonen-6-dithiohydrazide-1,9), occurs under these specific conditions when thiocarbohydrazide and propanone are the ligand synthons. 相似文献
2.
Oleg V. Mikhailov Marina A. Kazymova Tatyana A. Shumilova Galina A. Chmutova Svetlana E. Solovieva 《Transition Metal Chemistry》2005,30(3):299-304
The complexing process proceeding in the NiII–thiocarbohydrazide (H2N–H–NC(=S)–NH–NH2)–propanone triple system in EtOH solution and nickel(II)hexacyanoferrate(II) gelatin-immobilized matrix has been studied. It has been found that in the first case, template synthesis leading, as a minimum, to formation of three coordination compounds of NiII with (N,N,S,S)-donor tetradentate ligands having NiL1, NiL2 and NiL3compositions where L1 is 4,6,6-trimethyl-2,3,7,8-tetraazanonen-3-di(thiohydrazide)-1,9, L2 is 4,6,6,12-tetrametyl-1,9-dithio-2,3,7,8,10,11-hexaazatridekadien-3,11-hydrazide-1 and L3 is 2,8,10,10,16-pentamethyl-5,13-dithio-3,4,6,7,11,12,14,15-octaazaheptadekatrien-2,7,15 is observed, whereas in the gelatin-immobilized matrix, a complexing process in the system considered does not occur. 相似文献
3.
Oleg V. Mikhailov Marina A. Kazymova Tatyana A. Shumilova Galina A. Chmutova Svetlana E. Solovieva 《Transition Metal Chemistry》2005,30(1):18-21
The complexing processes in the M
II
-dithiomalonamide-diacetyl triple system (M=Ni, Cu) occuring in the nickel(II)- and copper(II)hexacyanoferrate(II) gelatin-immobilized matrix in contact with aqueous alkaline solutions (pH~12) containing dithiomalonamide and diacetyl at room temperature, and between MCl2, dithiomalonamide
and
diacetyl
in
EtOH
solutions
upon
heating
to$80°C, have been studied. In the Ni
II
-dithiomalonamide-diacetyl system, template synthesis occurs in EtOH solution but does not occur in the gelatin-immobilized matrix, whereas in the Cu
II
-dithiomalonamide-diacetyl system, template synthesis occurs in the gelatin-immobilized matrix but not in EtOH solution. Dithiomalonamide and diacetyl are the ligand synthons in the processes indicated. 相似文献
4.
The complexing processes in the CuII–1,2-diaminoethanedithione-1,2–ethanedione-1,2 and CuII–1,2-diaminoethanedithione-1,2–butanedione-2,3 triple systems occuring in the copper(II)hexacyanoferrate(II) gelatin-immobilized
matrix in contact with aqueous alkaline solutions (pH~12) containing 1,2-diaminoethanedithione-1,2 and ethanedione-1,2 or
butanedione-1,2 under room temperature, and between MCl2, 1,2-diaminoethanedithione-1,2 and ethanedione-1,2 or butanedione-1,2 in the ethanol solutions, upon heating up to ~80 °C,
have been studied. In both systems indicated, template synthesis occurs in the gelatin-immobililized matrix but does not occur
in the ethanol solution. As a result of template synthesis, macrocyclic CuII chelates with 2,7-dithio-3,6-diazaoctadien-3,5-dithioamide-1,8 and its 4,5-dimethylsubstituted derivative are formed in the
gelatin-immobililized matrix. 1,2-diaminoethanedithione-1,2 and ethanedione-1,2 or butanedione-2,3 are the ligand synthons
in the processes indicated. 相似文献
5.
O. V. Mikhailov M. A. Kazymova D. V. Chachkov 《Russian Journal of Inorganic Chemistry》2013,58(12):1518-1522
A new complexation process in the ternary system Ni(II)-hydrazinomethanethioamide (thiosemicarbazide)-2,3-butanedione (diacetyl) has been studied. Complexation occurs in an aqueous ethanol solution and in nickel(II) hexacyanoferrate(II) gelatin-immobilized matrix systems. It has been shown that, under these conditions, the process involves the “self-assembly” (template synthesis) of Ni(II) macrotricyclic complexes with a new chelating ligand—4,5-dimethyl-1,8-dimercapto-2,3,6,7-tetraaza-1,3,5,7-octatet-raene-1,8-diamine with the (NSSN) coordination of donor atoms to the metal atom. 相似文献
6.
M. A. Kazymova T. A. Shumilova O. V. Mikhailov S. E. Solov’eva 《Russian Journal of Coordination Chemistry》2008,34(2):102-105
Complexation in Cu2[Fe(CN)6]-gelatin-immobilized matrix implantates in contact with alkaline (pH > 10) aqueous solutions containing propane-1,3-dithioamide and butane-2,3-dione, as well as with an ethanolic solution containing the same organic compounds, was studied. It was found that room-temperature complexation in the gelatin matrix gives a macrocyclic complex CuL1with a tetradentate N,S,S,N-donor ligand via a template synthesis, while complexation in solution at room and higher temperatures yields only a bischelate Cu(II) complex with monodeprotonated propane-1,3-dithioamide. Schemes of the complexation processes were proposed. It was demonstrated that when propane-1,3-dithioamide and butane-2,3-dione are in direct contact in solution, the above N,S,S,N-donor ligand was formed in neither the presence nor the absence of Cu2+. 相似文献
7.
Complexation of CoIII, in the form of K[CoFe(CN)6]-gelatin-immobilized matrix, in contact with aqueous-alkaline solutions (pH ∼ 12) containing 1,2-diaminoethane-1,2-dithione
and propanone, has been studied. Template synthesis leading to a chelate CoIII coordination compound with a tetradentate N,N,S,S-donor ligand identified as 4,4,6-trimethyl-1,9-diamino-1,9-dimercapto-3,7-diazanon-3-en-2,8-dithione and hydroxy co-ligand
occurs under these specific conditions. 1,2-Diaminoethane-1,2-dithione and propanone are the ligand synthons in this process. 相似文献
8.
Complexing processes in systems containing NiII and 8-mercaptoquinoline or its derivatives (5-chloro-, 5-bromo-, 5-phenyl, 5-thiomethyl-8-mercaptoquinoline and 5,8-dimercaptoquinoline) take place in the nick- el(II)hexacyanoferrate(II) gelatin-immobilized matrix (GIM) in contact with an aqueous solution of the corresponding ligand. Under the conditions specified, in the NiII-8-mercaptoquinoline, NiII-5-chloro-8-mer captoquinoline,NiII-5-bromo-8-mercaptoquinoline, NiII-5-phenyl-8-mercaptoquinoline and NiII-5-thiomethyl-8-mercaptoquinoline systems, one water-insoluble complex of NiB2 composition (B– is a singly deprotonated ligand) is formed. In the NiII-5,8-dimercaptoquinoline system, two insoluble complexes, monomeric Ni(HB)2 and polymeric [Ni2B2(H2O)2]n (HB– is the singly, and B2– the doubly deprotonated form of the ligands) are generated. Upon complexing in solution or the solid phase, the formation of only one complex is observed in each of systems cited. 相似文献
9.
Novel complexing processes in the FeII-8-mercaptoquinoline, FeII-5-chloro-8-mercaptoquinoline and FeII-5-bromo-8-mercaptoquinoline systems, not used previously in coordination chemistry, namely complexing as an iron(III)hexacyanoferrate(II) gelatin-immobilized matrix (GIM) in contact with an aqueous solution of the corresponding ligand, have been observed and analysed. Incorporation of these ligands into the inner coordination sphere is preceded by the decomposition of the immobilized compound KFe[Fe(CN)6] to form hydroxides or oxohydroxides of FeII and FeIII under the action of OH- ions. It has been shown that FeIIFeIII redox process and the formation of FeB3 chelates (B- is a singly deprotonated form of the corresponding ligand) take place during complexing under such conditions. 相似文献
10.
Oleg V. Mikhailov Marina A. Kazymova Tatyana A. Shumilova Svetlana S. Solovieva 《Transition Metal Chemistry》2004,29(7):732-736
Novel complexing processes in the CuII-thiocarbohydrazide-diacetyl triple system proceeding to a copper(II)hexacyanoferrate gelatin-immobilized matrix system in contact with aqueous-alkaline (pH 12) solutions containing thiocarbohydrazide and diacetyl, have been studied. It has been shown that mild template synthesis of copper(II) coordination compounds with (N,S,N,S)- and (N,N,N,N)- tetradentate ligands - 4,5-dimethyl-2,3,6,7-tetraazaoctadien-3,5-dithiohydrazide-1,8 and 3,10-dithio--6,7,13,14-tetramethyl-1,2,4,5,8,9,11,12-octaazacyclotetradecatetraene-1,5,7,12 take place, respectively. At the same time, the complexing process in the system under examination, when it occurs in aqueous-ethanol solution between CuCl2 and the organic compounds indicated, leads to copper(II) coordination compounds with another (N,S,N,S)-tetradentate ligand - 3,9,10,16-tetramethyl-6,13--dimercapto-2,17-dioxo-4,5,7,8,11,12,14,15-tetraazaoctadecahexaene - 3,6,8,10,12,15. In both cases, thiocarbohydrazide and diacetyl are ligand synthons in these complexing processes. 相似文献