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Konarev DV Khasanov SS Otsuka A Yoshida Y Saito G 《Journal of the American Chemical Society》2002,124(26):7648-7649
The ionic multicomponent complex complex: ([Cr(I)(PhH)(2)].+))(2)[Co(II)TPP(C(60)(CN)(2))]-[C(60)(CN)(2)](.-).3(o-C(6)H(4)Cl(2)) (Co(II)TPP: cobalt (II) tetraphenylporphyrin; Cr(PhH)(2): bis(benzene)chromium; o-C(6)H(4)Cl(2): o-dichlorobenzene) containing CoTPP(C(60)(CN)(2)- anion and C(60)(CN)(2).- radical anion was obtained. The complex has the cage structure with channels, which accommodate Cr(I)(PhH)(2)(.+) and o-C(6)H(4)Cl(2) molecules. For the first time the sigma-bonding of Co(II)TPP to the fullerene radical anion with the essentially shortened Co.C(C(60)(CN)(2)) contact of 2.282 A is observed. The sigma-bonding results in the diamagnetism of Co(II)TPP(C(60)(CN)(2))(-) anion. The nonbonded C(60)(CN)(2)(.-) radical anion retains both the C(2)(v)symmetry and the shape of the molecule. The length of the C(triple bond)N bonds is 1.141 and 1.152 A. 相似文献
3.
A. A. Konarev 《Russian Journal of Applied Chemistry》2012,85(2):225-228
Possibility of using the electrodialytic method for purification of calcium gluconate to remove sodium bromide was examined.
The electrodialysis conditions were optimized. 相似文献
4.
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Dmitri V. Konarev Aleksey V. Kuzmin Salavat S. Khasanov Alexander F. Shestakov Akihiro Otsuka Hideki Yamochi Hiroshi Kitagawa Rimma N. Lyubovskaya 《化学:亚洲杂志》2020,15(17):2689-2695
Two salts of the aromatic hydrocarbon decacyclene, {cryptand[2.2.2](Cs+)} (decacyclene.?) ( 1 ) and {Bu3MeP+}(decacyclene.?) ( 2 ), were obtained. In both salts, decacyclene.? radical anions formed channels occupied by cations. However, corrugated hexagonal decacyclene.? layers could be outlined in the crystal structure of 1 with several side‐by‐side C???C approaches. The decacyclene.? radical anions showed strong distortion in both salts, deviating from the C3 symmetry owing to the repulsion of closely arranged hydrogen atoms and the Jahn‐Teller effect. Radical anions showed intense unusually low energy absorption in the IR‐range, with maxima at 4800 and 6000 cm?1. According to the carculations, these bands can originate from the SOMO‐LUMO+1 and SOMO‐LUMO+2 transitions, respectively. Radical anions exhibited a S=1/2 spin state, with an effective magnetic moment of 1.72 μB at 300 K. The decacyclene.? spin antiferromagnetically coupled with a Weiss temperature of ?11 K. Spin ordering was not observed down to 1.9 K owing to spin frustration in the hexagonal decacyclene.? layers. 相似文献
6.
A. S. Boikova Yu. A. D’yakova K. B. Il’ina P. V. Konarev A. E. Kryukova M. A. Marchenkova A. E. Blagov Yu. V. Pisarevskii M. V. Koval’chuk 《Crystallography Reports》2017,62(6):837-842
The composition of lysozyme solutions in D2O under conditions favorable for the formation of tetragonal crystals has been investigated at different protein concentrations by small-angle X-ray scattering using the synchrotron radiation. In addition to lysozyme monomers, dimeric and octameric species are found in the crystallization solutions; the octamer content increases with an increase in the protein concentration. A comparison of the data with those obtained under similar conditions but with H2O used as a solvent has shown that the replacement of light water with heavy one leads to increase of octamer volume fraction in solution. 相似文献
7.
Polarographic behavior of 2,4-dinitrobenzene and products of its reduction, 2-chloro-5-nitroaniline and 4-chloro-3-nitroaniline, is studied: it is shown that formation of the corresponding chloronitroanilines in the case of polarographic reduction of 2,4-dinitrochlorobenzene is rather problematic. 0.1 M NaOH is recommended as the supporting solution for analytical control of conversion of 2,4-dinitrochlorobenzene and a mixture of 2-chloro-5-nitroaniline and 4-chloro-3-nitroaniline in reaction solutions obtained by preparative electroreduction of 2,4-dinitrochlorobenzene. 相似文献
8.
Russian Journal of Electrochemistry - The electrochemical behavior of m-nitrosulphonic acid of benzene was studied by polarography, voltammetry at glassy carbon electrode, electrolysis at the... 相似文献
9.
Bronstein LM Shtykova EV Malyutin A Dyke JC Gunn E Gao X Stein B Konarev PV Dragnea B Svergun DI 《The journal of physical chemistry. C, Nanomaterials and interfaces》2010,114(50):21900-21907
Iron oxide nanoparticles (NPs) with a diameter 21.6 nm were coated with poly(maleic acid-alt-1-octadecene) (PMAcOD) modified with grafted 5,000 Da poly(ethyelene glycol) (PEG) or short ethylene glycol (EG) tails. The coating procedure utilizes hydrophobic interactions of octadecene and oleic acid tails, while the hydrolysis of maleic anhydride moieties as well as the presence of hydrophilic PEG (EG) tails allows the NP hydrophilicity. The success of the NP coating was found to be independent of the degree of grafting which was varied between 20 and 80% of the -MacOD-units, but depended on the length of the grafted tail. The NP coating and hydrophilization did not occur when the modified copolymer contained 750 Da PEG tails independently of the grafting degree. To explain this phenomenon the micellization of the modified PMAcOD copolymers in water was analyzed by small angle x-ray scattering (SAXS). The PMAcOD molecules with the grafted 750 Da PEG tails form compact non-interacting disk-like micelles, whose stability apparently allows for no interactions with the NP hydrophobic shells. The PMAcOD containing the 5,000 Da PEG and EG tails form much larger aggregates capable of an efficient coating of the NPs. The coated NPs were characterized using transmission electron microscopy, dynamic light scattering, ζ-potential measurements, and thermal gravimetry analysis. The latter method demonstrated that the presence of long PEG tails in modified PMAcOD allows the attachment of fewer macromolecules (by a factor of ~20) compared to the case of non-modified or EG modified PMAcOD, emphasizing the importance of PEG tails in NP hydrophilization. The NPs coated with PMAcOD modified with 60% (towards all -MAcOD- units) of the 5,000 PEG tails bear a significant negative charge and display good stability in buffers. Such NPs can be useful as magnetic cores for virus-like particle formation. 相似文献
10.
D. V. Konarev L. V. Zorina S. S. Khasanov E. U. Khakimova R. N. Lyubovskaya 《Russian Chemical Bulletin》2011,60(6):1063-1070
The ionic complexes simultaneously containing negatively charged coordination structures of metal phthalocyanines and fullerene anions, viz., {MnIIPc(CH3CH2S?) x ·(I?)1?x }·(C60 ·?)· ·(PMDAE+)2·C6H4Cl2 (PMDAE is N,N,N′,N′,N′-pentamethyldiaminoethane, x = 0.87, 1) and {ZnIIPc(CH3CH2S?)y·(I?)1?y }2·(C60 ?)2·(PMDAE+)4·(C6H4Cl2) (y = 0.5, 2) were synthesized. The both compounds were obtained as single crystals, which made it possible to study their crystal structures. In complex 1, the fullerene radical anions form honeycomb-like layers in which each fullerene has three neighbors with center-to-center interfullerene distances of 10.13–10.29 Å. Rather long distances between the C60 ·? radical anions results in the retention of monomeric C60 ·? in this complex down to the temperature of 110(2) K. In complex 2, fullerenes form dimers (C60 ?)2 bonded by one C-C bond. The dimers are packed in corrugated honeycomb-like layers with interfullerene center-to-center distances of 9.90–10.11 Å. Manganese(II) and zinc(II) phthalocyanines coordinate iodide and ethanethiolate anions to the central metal atom to form unusual negatively charged coordination structures MIIPc(An?) (An? is anion) packed in dimers {MIIPc(An?)}2 with a short distance between the phthalocyanine planes (3.14 Å in 1 and 3.27 Å in 2). The pthalocyanine dimers also form layers with the PMDAE+ cations, and these layers alternate with the fullerene layers. The packing of spherical fullerenes with planar phthalocyanine molecules is attained by the insertion of fullerenes between the phenylene groups of phthalocyanines. The π-π-interactions of the porphyrin macrocycle with five- or six-membered fullerene rings are characteristic of the earlier studied ionic porphyrin and fullerene complexes. Such interactions are not observed for ionic complexes 1 and 2. 相似文献