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61.
Vimlesh Chandra Rishi SrivastavaS. Sundar Manoharan 《Journal of magnetism and magnetic materials》2008
A series of nano-crystalline CoxAg100−x solid solutions have been prepared by NaBH4 reduction of the corresponding metal salts at room temperature in Ar gas flow. Alloys heat-treated at 600 °C in Ar/H2 (5%) show the evolution of metastable fcc Co precipitates in Ag. Magnetic studies indicate that all the compositions are ferromagnetic with Curie temperatures >400 K. For a nominal composition of Co60Ag40, heat-treated at 600 °C, an effective negative magneto-resistance (MR) ratio of the order of ∼21% at 350 K, at 2 T is observed. This could arise from the influence of magnetic field on the electron–phonon scattering effects near to Tc and to the spin-mixing scattering by magnons. 相似文献
62.
Rama Moorhy Appa S. Siva Prasad Jangam Lakshmidevi Bandameeda Ramesh Naidu Manchala Narasimhulu Katta Venkateswarlu 《应用有机金属化学》2019,33(10)
An agro waste‐derived, ‘water extract of pomegranate ash’ (WEPA), has been utilized for the first time as a renewable medium for Pd(OAc)2‐catalysed Suzuki–Miyaura cross‐coupling at room temperature. This method offers a simple and sustainable synthesis of biaryls from aryl halides and arylboronic acids under ligand‐ and external base‐free aerobic and ambient conditions. This method has been found effective for both activated and unactivated aryl halides in the production of biaryls with moderate to nearly quantitative yields. The protocol shows high chemoselectivity over identical/similar reactive sites in aryl halides (i.e. selectivity over identical halogens or different halogens of aryl halides). This method exhibits high regioselectivity, i.e. the selective reactivity of a halogen over other identical halogens at different positions on the aromatic nucleus. Therefore, we disclose here a clean, benign, substantial chemo‐ and regioselective and highly economic alternative method for the palladium‐assisted synthesis of biaryls using an agro waste‐derived medium. 相似文献
63.
Samir Kumar Sarkar Meenakshi Pegu Santosh Kumar Behera Siva Krishna Narra Pakkirisamy Thilagar 《化学:亚洲杂志》2019,14(24):4431-4431
64.
Dr. Siva Senthil Kumar Boominathan Kai-Hsin Chang Dr. Yu-Chiao Liu Chi-Shin Wang Cheng-Feng Wu Dr. Ming-Hsi Chiang Prof. Pi-Tai Chou Prof. Yao-Ting Wu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(30):7280-7284
Diindeno-fused dibenzo[a,h]anthracene 6 and diindeno-fused dibenzo[c,l]chrysene 9 contain the key moieties 1,4-quinodipropene (1,4-QDP) and 2,6-naphthoquinodipropene (2,6-NQDP), respectively, and they both have an open-shell singlet ground state. The latter compound exhibits a strong biradical character and interesting properties, including a low ΔET−S (2.44 kcal mol−1), a small HOMO–LUMO gap (1.06 eV), a wide photoabsorption range (250–1172 nm), and a large two-photon absorption cross-section (σ=1342±56 GM). This work verifies that 6 has a slightly larger HOMO–LUMO gap and ΔET−S than its helical isomer diindeno[2,1-f:1′,2′-j]picene (DIP), but is a much stronger two-photon absorber, verifying the important effect of geometry on the photophysical properties. 相似文献
65.
Samir Kumar Sarkar Meenakshi Pegu Santosh Kumar Behera Siva Krishna Narra Pakkirisamy Thilagar 《化学:亚洲杂志》2019,14(24):4588-4593
Typically, molecules with a twisted donor–acceptor (D‐A) architecture have been exploited for constructing thermally activated delayed fluorescence (TADF) materials. Herein, we report the first example of a thiophene‐based thermally activated delayed fluorescent molecule without a D‐A architecture. Compound 1 (2,5‐bis(2,2‐di(thiophen‐2‐yl)vinyl)thiophene) is conformationally flexible and shows weak fluorescence in the solution state but displays bright TADFin both condensed and solid states. Compound 1 crystallized in two different polymorphs ( 1 a and 1 b ). Interestingly, both polymorphs show distinctly different TADF features. The broad spectral features and the TADF characteristics of 1 have been explored for the time‐dependent multicolor (green, yellow and red) imaging of living cells. 相似文献
66.
Venkata Swamy Tangeti Kattaru Ramesh Babu G. V. Siva Prasad Tadikonda Ramu C. Venkata Rao 《Journal of the Iranian Chemical Society》2018,15(4):823-829
An efficient and rapid method was developed for the synthesis of C3-pyranopyrazole-substituted coumarins from one-pot five-component reaction of β-keto ester, hydrazine, O-hydroxy aromatic aldehydes, 6-methyl, 4-hydroxy pyranone and aromatic aldehyde in the presence of tri-ethylamine in solvent-free conditions. The microwave-assisted method reported herein offers advantageous shorter reaction times, higher yields and cleaner reaction compared with conventional heating methods. 相似文献
67.
P. Kuppusamy P. T. Manoharan C. Mahadevan M. Seshasayee 《Journal of chemical crystallography》1985,15(4):359-376
The crystal and molecular structure of the title compound, C21H11N6S4Ni, is reported. The crystals are triclinic:P¯1 (No. 2),Z=4,a=8.768(1),b=11.817(3),c=22.131(3) Å,=97.44(1),=91.90(1), and =94.04(1)°. The structure was solved by the heavy-atom method, and refined by full-matrix least squares toR=0.039 for 3213 unique reflections. The Ni atoms of both anions in the asymmetric unit have an approximately square-planar configuration. Anions and cations form segregated stacks alonga. The stacking of the anions along this direction is dimeric, with alternating Ni-Ni distances 4.111(2) and 7.593(2) Å for molecule I and 4.208(1) and 8.155(2) Å for molecule II. Static susceptibility measurements show strong antiferromagnetic coupling (2J=-241 cm–1) between the two anions of the dimers. 相似文献
68.
The total synthesis of (+)-(6R,2′S)-cryptocaryalactone and (−)-(6S,2′S)-epi cryptocaryalactone is reported based on stereoselective reduction of δ-hydroxy β-keto ester to install 1,3-polyol system, cis Wittig olefination, and lactonization as the key steps. The synthesis of (−)-(6S,2′S)-epi cryptocaryalactone is also reported using syn-benzylidene acetal formation and a preferential Z-Wittig olefination reaction and lactonization as the key steps. 相似文献
69.
Synthesis of novel 3-ary1-5-(3,5-dimethylisoxazol-4-y1)-2,3,5,6-tetrahydrobenzo[g][1,3,5]oxadiazocine-4-thiones 5 has been accomplished from 3,5-dimethylisoxazol-4-amine I by condensation with salicylaldehydes, followed by reduction, treatment with aryl isothiocyanates and subsequent smooth ring closure via acetal formation in the presence of formaldehyde. 相似文献
70.
Alabugin IV Timokhin VI Abrams JN Manoharan M Abrams R Ghiviriga I 《Journal of the American Chemical Society》2008,130(33):10984-10995
Despite being predicted to be stereoelectronically favorable by the Baldwin rules, efficient formation of a C-C bond through a 5-endo-dig radical cyclization remained unknown for more than 40 years. This work reports a remarkable increase in the efficiency of this process upon beta-Ts substitution, which led to the development of an expedient approach to densely functionalized cyclic 1,3-dienes. Good qualitative agreement between the increased efficiency and stereoselectivity for the 5-endo-dig cyclization of Ts-substituted vinyl radicals and the results of density functional theory analysis further confirms the utility of computational methods in the design of new radical processes. Although reactions of Br atoms generated through photochemical Ts-Br bond homolysis lead to the formation of cyclic dibromide side products, the yields of target bromosulfones in the photochemically induced reactions can be increased by recycling the dibromide byproduct into the target bromosulfones through a sequence of addition/elimination reactions at the exocyclic double bond. Discovery of a relatively efficient radical 5-endo-dig closure, accompanied by a C-C bond formation, provides further support to stereoelectronic considerations at the heart of the Baldwin rules and fills one of the last remaining gaps in the arsenal of radical cyclizations. 相似文献