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Institution

Indian Association for the Cultivation of Science

EducationKolkata, India
About: Indian Association for the Cultivation of Science is a education organization based out in Kolkata, India. It is known for research contribution in the topics: Excited state & Catalysis. The organization has 3867 authors who have published 10457 publications receiving 220098 citations.
Topics: Excited state, Catalysis, Ligand, Thin film, Band gap


Papers
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Journal ArticleDOI
TL;DR: In this article, the eigenvalue-independent partitioning (EIP) approach for the calculation of open-shell coupled cluster (CC) energy differences was used to compute the ionization potentials of HF and H 2 O using basis sets with and without polarization functions.

74 citations

Journal ArticleDOI
TL;DR: In this paper, a conjugated polymer was used to construct a NIR-active photovoltaic solar cell with high energy efficiency and short-circuit current (JSC) of 1.0 mA/cm2.

74 citations

Journal ArticleDOI
TL;DR: In this article, a single end-to-end bridging azido-bridged copper(II) 1D chain was obtained from condensation of pyridine-2-carbaldehyde with N, N-dimethylethane-1,2-diamine, N,N-diethylethanes-1.2-dimine, and 4-(2-aminoethyl)morpholine, respectively, and their crystal structures were determined by X-ray diffraction methods.
Abstract: Three new single end-to-end azido-bridged copper(II) chains [Cu(L1)(N3)]n(ClO4)n (1), [Cu(L2)(N3)]n(ClO4)n (2), and [Cu(L3)(N3)]n(ClO4)n (3) using three different tridentate Schiff bases L1, L2, and L3, obtained from condensation of pyridine-2-carbaldehyde with N,N-dimethylethane-1,2-diamine, N,N-diethylethane-1,2-diamine, and 4-(2-aminoethyl)morpholine, respectively, have been synthesized, and their crystal structures have been determined by X-ray diffraction methods. Complex 1, C10H15CuN6ClO4, crystallizes in an orthorhombic system, space group P212121, with a = 7.434(3), b = 12.047(4), c = 17.404(6) A, and Z = 4; complex 2, C12H19CuN6ClO4, crystallizes in an orthorhombic system, space group Pna21, with a = 14.723(5), b = 13.829(5), c = 8.002(5) A, and Z = 4 and complex 3, C12H17CuN6ClO5, crystallizes in an orthorhombic system, space group Pna21, with a = 13.837(15), b = 14.804(2), c = 8.050(4) A, and Z = 4. Each structure consists of a single end-to-end azido-bridged copper(II) 1D chain where each copper(II) center possesses a square pyramidal geometry. Magnetic susceptibility data, measured from 4 to 300 K, show weak ferromagnetic interaction through the end-to-end bridging azido pathway in all the complexes. The magnetic data were fitted to a high temperature series-expansion for a one-dimensional system with S = 1/2 local spin based on the Hamiltonian H = −JΣSi·Si+1 for all the complexes, giving the parameters J = +2.15 cm−1, g = 2.23 for 1, J = +3.61 cm−1, g = 2.16 for 2, and J = +2.06 cm−1, g = 2.17 for 3. This unusual magnetic behavior through the end-to-end bridging azido pathway has been correlated to the structural parameters. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

74 citations

Journal ArticleDOI
TL;DR: The effect of a room temperature ionic liquid (RTIL) on the conformational dynamics of a protein, human serum albumin (HSA), is studied by fluorescence correlation spectroscopy (FCS) and suggests recoiling of the unfolded protein by RTIL.
Abstract: The effect of a room temperature ionic liquid (RTIL) on the conformational dynamics of a protein, human serum albumin (HSA), is studied by fluorescence correlation spectroscopy (FCS). For this, the protein was covalently labeled by a fluorophore, 7-dimethylamino-3-(4-maleimidophenyl)-4-methylcoumarin (CPM). On addition of a RTIL ([pmim][Br]) to the native protein, the diffusion coefficient (Dt) decreases and the hydrodynamic radius (Rh) increases. This suggests that the RTIL ([pmim][Br]) acts as a denaturant when the protein is in the native state. However, addition of [pmim][Br] to a protein denatured by GdnHCl causes an increases in Dt and decrease in Rh. This suggests that in the presence of GdnHCl addition of RTIL helps the protein to refold. In the native state, the conformational dynamics of protein is described by three distinct time constants: ∼3.6 ± 0.7, ∼29 ± 4.5, and 133 ± 23 μs. The faster components (∼3.6 ± 0.7 and ∼29 ± 4.5 μs) are ascribed to chain dynamics of the protein, while the slowest...

74 citations

Journal ArticleDOI
TL;DR: Diffusion of organic dyes in neat room temperature ionic liquid (RTIL) and RTIL-mixed micelle has been studied by fluorescence correlation spectroscopy (FCS) and suggests very high viscosity of the RTILs.
Abstract: Diffusion of organic dyes in neat room temperature ionic liquid (RTIL) and RTIL-mixed micelle has been studied by fluorescence correlation spectroscopy (FCS). We have selected two RTILs, 3-pentyl-1-methyl imidazolium bromide ([C5C1Im][Br]) and the corresponding tetra-fluoroborate ([C5C1Im][BF4]). Diffusion coefficients (Dt) of three organic dyes—DCM (neutral), C480 (neutral), and C343 (anionic)—in these RTILs are ∼100 times slower compared to water. This indicates very high viscosity of the RTILs. In contrast to water, the Dt in RTIL exhibits a wide distribution which suggests the presence of heterogeneity (nanoscale organization). The presence of ions in the RTILs markedly affects diffusion in the RTILs. Dt's of C480 (neutral) and C343 (anionic) are very similar in water but in RTILs the ionic dye C343 diffuses 1.7 times slower than neutral C480. This is attributed to the electrostatic force exerted by the ions in the RTILs. In the giant (∼2–4 μm) [C5C1Im][Br]-triblock copolymer (P123) mixed micelle Dt o...

74 citations


Authors

Showing all 3900 results

NameH-indexPapersCitations
Yves Pommier12378958898
Flemming Besenbacher11472851827
Katsuhiko Ariga11286445242
Shunichi Fukuzumi111125652764
Rajdeep Mohan Chatterjee11099051407
Kwang S. Kim9764262053
Amar K. Mohanty8153831856
Nigel D. Browning8164623621
Andrea Caneschi8043525896
Rodolphe Clérac7850622604
Subrata Ghosh7884132147
Miaofang Chi7730422817
Yuan Ping Feng7765025846
D. D. Sarma7052118082
Asim Bhaumik6946616882
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202310
202283
2021443
2020447
2019452
2018467