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131.
S. K. Ghosh E. Tettamanti P. L. Indovina 《Zeitschrift für Physik B Condensed Matter》1976,24(2):227-233
Contributions to the spin-lattice relaxation time (T
1) and the spin-spin relaxation time (T
2) due to critical fluctuations (CF) have been determined in para-azoxyanisole (PAA) from the corresponding proton relaxation times measured at 60 MHz over a temperature range of about 35 °K above the nematic-isotropic transition temperatureT
C
.In determining the CF contributions, the procedure followed here is the same as the present authors used earlier for a similar study in p-methoxybenzylidene p-n butylaniline (MBBA). Like that in MBBA at 14 MHz, a maximum in the CF contribution toT
1, has been observed. Following a recent theory we identify this contribution toT
1 arising from the nonlocal part of CF, and we call thisT
1)CFN. The correlation time associated with this nonlocal part of CF,
CFN, has been determined at different temperatures fromT
1)CFN. The temperature dependence of
CFN is in good agreement with the Landau-de Gennes theory and is consistent with that observed earlier in MBBA. The temperature dependence ofT
2)CF is also in reasonable agreement with the above behavior of
CFN. However, ourT
2)CF data can also be fitted to a temperature dependence expected from a contribution toT
2)CF arising from the local part of CF, such a fitting is comparatively poorer than the former. Since ourT
2)CF data are neither sufficiently accurate nor elaborate, no attempt has been made here to separate these two contributions, nonlocal and local parts of CF, which have been predicted from theoretical considerations. A behavior similar to that of ourT
2)CF is also shown by the earlier data of Cabane and Clark obtained from14N resonance when their data are processed properly.Work done with the financial support of the Consiglio Nazionale delle Ricerche granted through the Gruppo Nazionale di Struttura della Materia to the Istituto di Fisica, Università dell' AquilaA preliminary report of this work was presented at the Fifth International Symposium on Magnetic Resonance held at Bombay, India, January 14–18, 1974 相似文献
132.
Reactivity of [M2(μ‐Cl)2(cod)2] (M=Ir,Rh) and [Ru(Cl)2(cod)(CH3CN)2] with Na[H2B(bt)2]: Formation of Agostic versus Borate Complexes
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K. Bakthavachalam K. Yuvaraj Mohammad Zafar Prof. Dr. Sundargopal Ghosh 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(48):17291-17297
Treatment of [M2(μ‐Cl)2(cod)2] (M=Ir and Rh) with Na[H2B(bt)2] (cod=1,5‐cyclooctadiene and bt=2‐mercaptobenzothiazolyl) at low temperature led to the formation of dimetallaheterocycles [(Mcod)2(bt)2], 1 and 2 ( 1 : M=Ir and 2 : M=Rh) and a borate complex [Rh(cod){κ2‐S,S′‐H2B(bt)2}], 3 . Compounds 1 and 2 are structurally characterized metal analogues of 1,5‐cyclooctadiene. Metal–metal bond distances of 3.6195(9) Å in 1 and 3.6749(9) Å in 2 are too long to consider as bonding. In an attempt to generate the Ru analogue of 1 and 2 , that is [(Rucod)2(bt)2], we have carried out the reaction of [Ru(Cl)2(cod)(CH3CN)2] with Na[H2B(bt)2]. Interestingly, the reaction yielded agostic complexes [Ru(cod)L{κ3‐H,S,S′‐H2B(bt)2}], 4 and 5 ( 4 : L=Cl; 5 : L=C7H4NS2). One of the key differences between 4 and 5 is the presence of different ancillary ligands at the metal center. The natural bond orbital (NBO) analysis of 1 and 2 shows that there is four lone pairs of electrons on each metal center with a significant amount of d character. Furthermore, the electronic structures and the bonding of these complexes have been established on the ground of quantum‐chemical calculations. All of the new compounds were characterized by IR, 1H, 11B, 13C NMR spectroscopy, and X‐ray crystallographic analysis. 相似文献
133.
134.
135.
Koushik Saha Benson Joseph Rongala Ramalakshmi Dr. R. S. Anju Dr. Babu Varghese Prof. Sundargopal Ghosh 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(23):7871-7878
Thermolysis of [Cp*Ru(PPh2(CH2)PPh2)BH2(L2)] 1 (Cp*=η5‐C5Me5; L=C7H4NS2), with terminal alkynes led to the formation of η4‐σ,π‐borataallyl complexes [Cp*Ru(μ‐H)B{R‐C=CH2}(L)2] ( 2 a – c ) and η2‐vinylborane complexes [Cp*Ru(R‐C=CH2)BH(L)2] ( 3 a – c ) ( 2 a , 3 a : R=Ph; 2 b , 3 b : R=COOCH3; 2 c , 3 c : R=p‐CH3‐C6H4; L=C7H4NS2) through hydroboration reaction. Ruthenium and the HBCC unit of the vinylborane moiety in 2 a – c are linked by a unique η4‐interaction. Conversions of 1 into 3 a – c proceed through the formation of intermediates 2 a – c . Furthermore, in an attempt to expand the library of these novel complexes, chemistry of σ‐borane complex [Cp*RuCO(μ‐H)BH2L] 4 (L=C7H4NS2) was investigated with both internal and terminal alkynes. Interestingly, under photolytic conditions, 4 reacts with methyl propiolate to generate the η4‐σ,π‐borataallyl complexes [Cp*Ru(μ‐H)BH{R‐C=CH2}(L)] 5 and [Cp*Ru(μ‐H)BH{HC=CH‐R}(L)] 6 (R=COOCH3; L=C7H4NS2) by Markovnikov and anti‐Markovnikov hydroboration. In an extension, photolysis of 4 in the presence of dimethyl acetylenedicarboxylate yielded η4‐σ,π‐borataallyl complex [Cp*Ru(μ‐H)BH{R‐C=CH‐R}(L)] 7 (R=COOCH3; L=C7H4NS2). An agostic interaction was also found to be present in 2 a – c and 5 – 7 , which is rare among the borataallyl complexes. All the new compounds have been characterized in solution by IR, 1H, 11B, 13C NMR spectroscopy, mass spectrometry and the structural types were unequivocally established by crystallographic analysis of 2 b , 3 a – c and 5 – 7 . DFT calculations were performed to evaluate possible bonding and electronic structures of the new compounds. 相似文献
136.
A new and efficient synthesis has been developed for the title indolocarbazole which has been indicated by a recent computer-aided study to be a potent ligand for the receptor for the naturally occurring carcinogen, TCDD. 相似文献
137.
Various nitroarenes and 2,1,3-benznooxadiazole-1-oxides were selectively and rapidly reduces to their corresponding amino and diamino compounds respectively in high yields using (NH4SO4-Mg/A1/Bi, a new reduction system. 相似文献
138.
In this paper we have proposed a technique based on image analysis of the surface plasmon excitation at the metal-dielectric interface of inside silver coated fused silica capillary glass tube. Chemical deposition technique has been used for the deposition of silver. Angular interrogation in Kretschmann-like configuration is realized by non-radial transverse illumination of this cylindrical dielectric-metal-dielectric (C-DMD) structure with a He–Ne laser source. Here the uniform film deposition of the inside surface of the capillary is not that crucial except within the transversely illuminated working area concerned. Moreover, the proposed technique has been validated experimentally for sensing different aqueous dielectric samples inserted inside the tube. 相似文献
139.
140.
Ovender Singh Priyanka Gupta Anshu Singh Ankur Maji Udai P. Singh Kaushik Ghosh 《应用有机金属化学》2019,33(5)
Hexacoordinated non‐heme iron complexes [FeII(L1)2](ClO4)2 ( 1 ) and [FeII(L2)2](PF6)2 ( 2 ) have been synthesized using ligands L1 = (E)‐2‐chloro‐6‐(2‐(pyridin‐2ylmethylene) hydrazinyl)pyridine and L2 = (E)‐2‐chloro‐6‐(2‐(1‐(pyridin‐2‐yl)ethylidene)hydrazinyl) pyridine]. These complexes are highly active non‐heme iron catalysts to catalyze the C (sp3)?H bonds of alkanes. These iron complexes have been characterized using ESI?MS analysis and molecular structures were determined by X‐ray crystallography. ESI ? MS analysis also helped to understand the generation of intermediate species like FeIII?OOH and FeIV=O. DFT and TD?DFT calculations revealed that the oxidation reactions were performed through high‐valent iron center and a probable reaction mechanism was proposed. These complexes were also utilized for the degradation of orange II and methylene blue dyes. 相似文献