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91.
Kuno Wagner Kurt Findeisen Walter Schfer Werner Dietrich 《Angewandte Chemie (International ed. in English)》1981,20(10):819-830
Research in the field of low-molecular weight, oligomeric and polymeric α,ω-diisocyanatocarbodiimides and -polycarbodiimides has been fruitful, not only in connection with these compounds themselves, but also—as so often happens in chemistry—with quite different problems. Novel synthetic methods, discoveries concerning the properties of low-molecular weight carbodiimides and phosphane imide derivatives, as well as results on the fragmentation reactions of four-membered heterocyclic compounds containing oxygen, phosphorus, and nitrogen, and a better understanding of the diisocyanate polyaddition process are among the many by-products of this research. The “high- and low-temperature formation” of polycarbodiimides and the homogeneous and heterogeneous catalysis of this process are described, and the fundamental importance of four-membered ring fragmentation mechanisms resulting in the formation of phosphane imide derivatives is outlined. Interesting building blocks for the diisocyanate polyaddition and polycondensation processes can be synthesized by many derivatization reactions of oligomeric and high-molecular weight polycarbodiimides and polyuretonimines. The in situ production of polycarbodiimides via matrix reactions in flexible polyurethane foams leads to a cellular arrangement of the material due to the pronounced symmetrical growth processes. Combination-foams with increased carbonation tendencies are formed in this way. Attention is drawn to several industrial applications of α,ω-diisocyanatopolycarbodiimides, of high-molecular weight cross-linked polyuretonimines, and of polycarbodiimide foams. 相似文献
92.
Gaseous Complexes NiAl2Cl8 and NiAl3Cl11 Spectral photometric measurements of equilibria which are established by reaction of solid NiCl2 with gaseous Al2Cl6 have been made. Results see ?Inhaltsübersicht”?. 相似文献
93.
Di-lithiated octamethylcyclotetrasilazane (OMCTS, 1) reacts with halosilanes in different ways. Ring contraction with formation of the isomeric cyclodisilazanes 2, 3 occurs in the reaction with chloro- and fluorotrimethylsilanes. Substitution (6) and ring contraction with formation of the isomeric six-membered ring 7 occurs with chlorodimethylsilane. 2, 3, 6 and 7 are excellent precursors of silyl-bridged, SiH-functional, four-membered ring systems (4, 5, 9–11). The mechanism of the isomerization reactions are discussed. 相似文献
94.
Abstract— The photobehavior of the ciliates Climacostomuum virens, Euplotes daidaleos and Paramecium bursaria associated with endosymbiotic green algae ( Chlorella sp.) was compared with that of aposymbiotic ciliates (ciliates free of algae) and with the always aposymbiotic Paramecium arcticum . The aposymbiotic ciliates showed step-up photophobic responses. The responses were more frequent and occurred at lower light intensities when the organisms contained endosymbiotic algae. In contrast, step-down photophobic responses and photoaccumulations, as well as photokinesis, were never observed in aposymbiotic cells. These responses could be found only in ciliates when endosymbionts were present with the exception of C. virens , which showed none of these photoresponses. 相似文献
95.
Me3B3N3H3Cr(CO)3 has been obtained by ring-ligand exchange starting from Et3B3N3Me3Cr(CO)3 and Me3B3N3H3. The new compound has been characterised by means of their IR, NMR, UV and mass spectroscopic data. 相似文献
96.
Werner Kutzelnigg 《Chemical physics》1978,28(3):293-298
Necessary conditions are derived that a symmetry-adapted perturbation theory for intermolecular forces (exchange perturbation theory) has to satisfy and which is essentially a condition for the existence of the primitive function Φ. The concept of a “genuine primitive function” is introduced and it is shown that the Φ of the AM, EL-HAV AND MS-MA schemes is not a genuine primitive function whereas that of the HS scheme is. 相似文献
97.
Open- and closed-shell states in few-particle quantum mechanics. II. Classification of atomic states
The system developed in the first paper of this series for the classification of states as open- or closed-shed type is applied to atomic states. These may be classified in the isoelectronic limit (Z → ∞) from knowledge of the true wave function in this limit. One-matrix occupation numbers are tabulated for a number of states of the first-row atoms in the limit Z → ∞ and the states classified. A classification for finite Z is possible in the framework of the Z-dependent perturbation theory by use of a thoerem for the stability of a closed-shed with respect to small perturbations. Such a stability does not hold in general for open-shel states. 相似文献
98.
99.
A simple semiconductor gas sensor (TGS 812) is used for the on-line measurement and control of indole during the production of l-tryptophan from indole and l-serine with immobilized E. coli cells. Indole is estimated in the reactor gas space. In combination with an automatic indole supply system, a feed-batch process became possible. The indole concentration was monitored and kept within the optimal range (300–600 mg l?1). A simple gas-sensing electrode dipped in the reaction medium provides direct measurement of organic solvents and gases in the liquid. Such a system is suitable for on-line determination of ethanol (10–70 g l?1) during continuous production of ethanol with immobilized yeast cells. 相似文献
100.
The complex [C5H5RhH(C2H4)PMe3]BF4 (I) reacts with NaF and NaCN by deprotonation to give C5H5Rh(PMe3)C2H4 but with NaCl, NaBr and NaI the ethylrhodium compounds C5H5RhC2H5(PMe3)X (II–IV) are obtained. The reactions of I with CO and PPri3 yield the BF4 salts of the cations [C5H5RhH(CO)PMe3]+ and [C5H5RhH(PPri3)PMe3]+ (V, VI), respectively, from which the uncharged complexes C5H5Rh(CO)PMe3 (VII) and C5H5Rh(PPRi3)PMe3 (VIII) are prepared. The carbonyl compound VII is also accessible either from C5H5Rh(CO)2 and PMe3 or from C5H5Rh(PMe3)2 and CO. The reaction of I with ethylene leads to the BF4 salt of the cation [C5H5RhC2H5(PMe3)C2H4]+ (X) which on treatment with PMe3 forms the complex [C5H5RhC2H5(PMe3)C2H4PMe3]BF4 (XI). The compound [C5H5RhH(C2H4)PPri3]BF4 (XII) reacts with NaI by insertion to yield C5H5RhC2H5(PPri3)I (XIII) whereas with PPri3 the salt [C5H5RhH(PPri3)2]BF4 (XIV) is produced. The bis(triisopropylphosphine) complex C5H5Rh(PPri3)2 (XVI) is obtained from XIV and NaH. 相似文献