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T. V. Ramakrishnan H. R. Krishnamurthy S. R. Hassan G. Venketeswara Pai 《Journal of Chemical Sciences》2003,115(5-6):767-774
Manganites of the LA1−x
Ca
x
MnO3 family show a variety of new and poorly understood electronic, magnetic and structural effects. Here we outline a new approach
recently proposed by us, where we argue that due to strong Jahn-Teller (JT) coupling with phonons the twofold degeneratee
g
states at the Mn sites dynamically reorganize themselves into localised, JT polaronsl with exponentially small inter-site hopping, and band-like, nonpolaronic statesb, leading to anew 2-band model for manganites which includes strong Coulomb and Hund’s couplings. We also discuss some results from a dynamical mean-field theory treatment
of the model which explains quantitatively a wide variety of experimental results, including insulator-metal transitions and
CMR, in terms of the influence of physical conditions on the relative energies and occupation of thel andb states. We argue that this microscopic coexistence of the two types of electronic states, and their relative occupation and
spatial correlation is the key to manganite physics.
Dedicated to Professor C N R Rao on his 70th birthday 相似文献
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S. S. Krishnamurthy P. Ramabrahmam A. R. Vasudeva Murthy R. A. Shaw M. Woods 《无机化学与普通化学杂志》1985,522(3):226-234
The reactions of pentachloro(2′, 2′, 2′-triphenylphosphazen-1′-yl)cyclotriphosphazene, N3P3Cl5(NPPh3), with primary and secondary amines have been investigated using diethyl ether, methyl cyanid or benzene as the solvent. The structures of the products obtained, N3P3Cl5minus;nRn(NPPh3) [n = 1, R = NHMe, NHBut, NMe2, NC5H10, NEt2; n = 2, R = NMe2, NC5H10, NEt2; n = 3, R = NMe2, NHBut; n = 5, R = NMe2] are elucidated by 1H and 31P NMR spectroscopy. The ? NPPh3 substituent exerts a pronounced geminal directing influence on incoming secondary amino nucleophiles; compounds containing a ≡ PCl(NPPh3) group are not formed at the bis and subsequent stages of chlorine replacement. The reactions that involve primary amines follow the pattern established for the analogous reactions of hexachlorocyclotriphosphazene. The effect of solvent and possible mechanism(s) are discussed. 相似文献
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[chemical reaction: see text]. Direct addition of Grignard reagents to acid chlorides in the presence of bis[2-(N,N-dimethylamino)ethyl] ether proceeds selectively to provide aryl ketones in high yields. A possible tridentate interaction between Grignard reagents and bis[2-(N,N-dimethylamino)ethyl] ether moderates the reactivity of Grignard reagents, preventing the newly formed ketones from nucleophilic addition by Grignard reagents. 相似文献
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A new and efficient synthesis of benzof'uro[3,2-b]quinolin-6(11H) one ( 3 ) is reported, by treatment of 2- {[(phenoxy)acetyl]amino} benzoic acid ( 6a ) with polyphosphoric acid. An intermediate in the conversion of 3 to 6a , namely, 2-(3-benzofuranylamino)benzoic acid ( 7 ), was defined. An improved method for the synthesis of 6a is also described, which was used to prepare analogs ( 6b-n ) of 6a . In addition, an 11-alkoxy derivative ( 8 ) and 11-dialkylamino derivatives ( 10 and 11 ) of benzofuro [3,2-b]quinoline were prepared from 3 . 相似文献
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Yang J Gitlin I Krishnamurthy VM Vazquez JA Costello CE Whitesides GM 《Journal of the American Chemical Society》2003,125(41):12392-12393
Proteins are functional biopolymers; viewed as molecules, they are also monodisperse polyamides with chemically reactive side chains. This paper describes the use of proteins as starting materials for the synthesis of monodisperse polymers with nonbiological functionalities attached to the side chains. It demonstrates the complete derivatization of amine groups (lysine side chains and N-termini) on three different proteins by addition of activated carboxylate reagents in aqueous solutions containing sodium dedecyl sulfate (SDS), under denaturing conditions. Several different acylating reagents were used to generate derivatized proteins; the resulting compounds constitute a new class of monodisperse, semisynthetic polymers, having the potential for wide variation in the structure of the backbone and of the side chains. Modification of lysozyme on a gram scale demonstrated that the method can generate useful quantities of material. 相似文献
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