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971.
G. Merle J. P. Pascault Q. T. Pham C. Pillot R. Salle J. Gol I. Rashkov I. Panayotov D. Gurard A. Hrold 《Journal of polymer science. Part A, Polymer chemistry》1977,15(9):2067-2074
In the present work, we use the binary insertion compound LiC12 to polymerize styrene, methyl methacrylate, butadiene, isoprene, and to copolymerize isoprene and styrene in various hydrocarbon solvents (aromatics and aliphatic) and etheral solvents. We show that the styrene polymerization in aromatic solvents gives better yields than in the etheral solvents, the polymer being atactic. Methyl methacrylate does not polymerize in toluene but does so completely in DME. More generally, the yields of polymerization are better with KC37 than with LiC12 because of the different capacities of the monomer to get into the carbon layers. The polymerization of dienes with LiC12 shows that the microstructures of the polymer obtained in π-or n-donor solvents are similar to the ones obtained by homogenous polymerization with Li cation in such solvents. However, for isoprene in cyclohexane, the results are different. The isoprene styrene copolymers are statistical ones and the mean length of styrene blocks is less than 5. The monomer interaction with the insertion compound and the growing chain geometry between the carbon layers are the facts which control either the stereospecificity of the polymerization or the selectivity of the copolymerization. 相似文献
972.
973.
Conclusions The complexes of Co, Ni, Fe, and Cu with dimethyl- and diphenylglyoxime inhibit the initiated oxidation of cumene by reacting with the peroxide radicals.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1342–1344, June, 1971. 相似文献
974.
975.
In this paper, the NO-to-NO
2
conversion in various gaseous mixtures is experimentally investigated. Streamer coronas are produced with a dc-superimposed high-frequency ac power supply (10–60 kHz). According to NO
x
removal experiments in N
2
+NO
x
and N
2
+O
2
+NO
x
gaseous mixtures, it is supposed that the reverse reaction NO
2
+ONO+O
2
may not only limit NO
2
production in N
2
+NO
x
mixtures, but also increase the energy cost for NO removal. Oxygen could significantly suppress reduction reactions and enhance oxidation processes. The reduction reactions, such as N+NON
2
+O, induce negligible NO removal provided the O
2
concentration is larger than 3.6%. With adding H
2
O into the reactor, the produced NO
2
per unit removed NO can be significantly reduced due to NO
2
oxidation. NH
3
injection could also significantly decrease the produced NO
2
via NH and NH
2
- related reduction reactions. Almost 100% of NO
2
can be removed in gaseous mixtures of N
2
+O
2
+H
2
O+NO
2
with negligible NO production. 相似文献
976.
S. D. Mikhano N. S. Kulachkina T. M. Filippova I. G. Suchkova V. M. Berezovskii 《Chemistry of Natural Compounds》1981,17(2):176-178
(±)-Biotin has been synthesized from a mixture of cis- and allo-trisubstituted dehydrothiophanes by a scheme providing for the easy elimination of the accompanying allo-substituted thiophane in the form of an intermediate and not as the final isomeric allo-biotin. The imidazoline ring of biotin is formed from a dialkoxy-carbonyldiaminothiophane under the conditions of partial hydrolysis of one of the protective groups with the elimination of phosgene from the scheme of synthesis.All-Union Scientific-Research Vitamin Institute, Moscow. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 220–223, March–April, 1981. 相似文献
977.
978.
979.
Photoinduced electron transfer (PET) fluoroionophores (1b, 2b) that consist of diazacrown and two 9-anthryl pendants show fluorescent enhancement with various guest salts. The diaza-12-crown-4 derivative (2b) exhibited Zn(2+) selectivity and in the presence of this cation the host fluorescence intensity was increased by a factor of 182. The guest cation-induced fluorescence enhancement of 2b was larger than the diaza-18-crown-6 derivative (1b). 相似文献
980.
The present state of a long term program is reviewed. It was started to elaborate a remote controlled automated radiochemical
processing system for the neutron activation analysis of biological materials. The system is based on wet ashing of the sample,
followed by reactive desorption of some volatile components. The distillation residue is passed through a series of columns
filled with selective ion screening materials to remove the matrix activity. The solution is thus “stripped” from the interfering
radioions, and it is processed to single-elements through group separations using ion-exchange chromatographic techniques.
Some special problems concerning this system are treated. (a) General aspects of the construction of a (semi)automated radiochemical
processing system are discussed; (b) Comparison is made between various technical realizations of the same basic concept;
(c) Some problems concerning the “reconstruction” of an already published processing system are outlined. 相似文献