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1.
Das Pritam Kumar Mallik Arnab Kumar Molla Altaf Hossain Santra Apurba Kumar Ganguly Ranjan Saha Abhijit Kumar Sugam Aswal V. K. 《Journal of Thermal Analysis and Calorimetry》2022,147(10):5617-5635
Journal of Thermal Analysis and Calorimetry - Nanofluids have gained recent attention because of their potential applications in diverse engineering fields like enhancing thermal transport,... 相似文献
2.
Xiao Huang Bishwa Ranjan Nayak Tao Lu Lowe 《Journal of polymer science. Part A, Polymer chemistry》2004,42(20):5054-5066
A series of novel multifunctional hydrogels that combined the merits of both thermoresponsive and biodegradable polymeric materials were designed, synthesized, and characterized. The hydrogels were copolymeric networks composed of N‐isopropylacrylamide (NIPAAM) as a thermoresponsive component, poly(L‐lactic acid) (PLLA) as a hydrolytically degradable and hydrophobic component, and dextran as an enzymatically degradable and hydrophilic component. The chemical structures of the hydrogels were characterized by an attenuated total reflection–Fourier transform infrared spectroscopy (ATR–FTIR) technique. The hydrogels were thermoresponsive, showing a lower critical solution temperature (LCST) at approximately 32 °C, and their swelling properties strongly depended on temperature changes, the balance of the hydrophilic/hydrophobic components, and the degradation of the PLLA component. The degradation of the hydrogels caused by hydrolytic cleavage of ester bonds in the PLLA component was faster at 25 °C below the LCST than at 37 °C above the LCST, determined by the ATR–FTIR technique. Due to their multifunctional properties, the designed hydrogels show great potential for biomedical applications, including drug delivery and tissue engineering. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5054–5066, 2004 相似文献
3.
Some bounds on the entries and on the norm of the inverse of triangular matrices with nonnegative and monotone entries are found. All the results are obtained by exploiting the properties of the fundamental matrix of the recurrence relation which generates the sequence of the entries of the inverse matrix. One of the results generalizes a theorem contained in a recent article of one of the authors about Toeplitz matrices. 相似文献
4.
Paital AR Mitra T Ray D Wong WT Ribas-Ariño J Novoa JJ Ribas J Aromí G 《Chemical communications (Cambridge, England)》2005,(41):5172-5174
Based on a combined theoretical-experimental study, we propose that substituted m-phenylene ligands (m-N-Phi-N) can act as tuneable strong ferromagnetic couplers connecting Cu(II) ions; a new complex presenting that bridge with J close to +15 cm(-1) has been suggested and synthesized. 相似文献
5.
We present exact explicit expressions for the row spin-spin correlation functions
00
n0 in the isotropicd= 2 Ising model, in terms of elliptic integrals, forn 5. We also give a general structural formula for
00
n0. 相似文献
6.
Photoaffinity labeled (3-diazoacetoxy)-9-cis-retinal (1) and (9-methylenediazoacetoxy)-9-cis-retinal (20) were synthesized and bound to absorption maxima at 465 and 460 nm respectively. Binding studies established that synthetic retinals 1 and 2 bind to the natural binding site and that the integrity of the diazoacetoxy photoaffinity label is preserved in the process. Incorporation of 3-(O14COCHN2)-labeled 9-cis retinal could be conveniently carried out in high yield using apomembrane solubilized in CHAPS as detergent to afford the pigment analog in a pure form. Photolysis of the diazoacetoxy group within the binding site led to 15–20%, crosslinking of rhodopsin as estimated by using radiocarbon containing labeled retinal 1 thus showing that this synthetic retinal is suitable for photoaffinity labeling of the active site in rhodopsin. Subsequent experiments to establish the site(s) of crosslinking by sequencing studies will then contribute to our knowledge of the structure of rhodopsin. 相似文献
7.
Valeria Balogh-Nair John D. Carriker Barry Honig Vinayak Kamat Michael G. Motto Koji Nakanishi Ranjan Sen Mordechai Sheves Maria Arnaboldi Tanis Kazuo Tsujimoto 《Photochemistry and photobiology》1981,33(4):483-488
Abstract— The difference (in cm−1 ) in absorption maxima between the protonated Schiff base of retinals and the pigment derived therefrom has been defined as the opsin shift. It represents the influence of the opsin binding site on the chromophore. The analysis of the opsin shifts of a series of dihydrobacteriorhodopsins has led to the external point-charge model, which in addition to a counter anion near the Schiff base ammonium, carries another negative charge in the vicinity of the β-ionone ring. This is in striking contrast to the external point-charge model proposed earlier for the bovine visual pigment. The absorption maxima of rhodopsins formed from bromo- and phenyl retinals support the two models. A retinal carrying a photoaffinity label has yielded a nonbleachable bacteriorhodopsin. 相似文献
8.
Minimizing molecular mobility for desiccation preservation of biologics close to ambient temperature using trehalose glasses require quantitative characterization of their enthalpic relaxation at various end water contents. Differential scanning calorimetry (DSC) was used to characterize three different water contents: 0%, 1.5% and 10% over a wide range of aging temperatures. Results showed the characteristic time (τ) varies both with the water content and the aging temperature. τ increased with lowered aging temperature but showed a non-monotonous relationship as a function of water content. Fragility of trehalose glasses was analyzed using thermophysical parameters obtained from relaxation studies. The study showed trehalose to be a fragile glass former at all water contents, with 0% water samples showing a relatively stronger glass. A compromise between molecular mobility and glass fragility led to an optimal water content close to 1.5% and an aging temperature close to room temperature. This would ensure a τ value of 9000 h, which corresponds to a storage period of a year. 相似文献
9.
Frank G. Riddell Eric S. Turner Alan R. Katritzky Ranjan C. Patel Fernando M.S. Brito-Palma 《Tetrahedron》1979,35(11):1391-1398
The synthesis and variable temperature 1H and 13C NMR spectra of three tetrahydro-1,2,4-oxadiazines are reported. The N(4)-Me inversion barriers are 6.8–7.0 (ax→ts) and 7.4–7.9 kcal mol?1 (eq→ts) with ΔG° 0.6–0.9 kcal mol?1. The N(2)-Me inversion barriers are 10.4–11.4 (ax→ts) and 11.6–13.1 kcal mol?1 (eq→ts) with ΔGδ 1.2–1.7 kcal mol?1. The barrier to ring inversion is ca. 12.7 kcal mol?1. “R value” analysis shows the ring to have a 56.5±2δ dihedral angle about the C(5)-(6) bond, indicative of the expected chair conformation. 相似文献
10.
[VIVO(acac)2] reacts with the methanolic solutions of tridentate dibasic ONO donor hydrazone ligands derived from the condensation of
benzoyl hydrazine with either 2-hydroxyacetophenone (H2L1) or its para-substituted derivatives (H2L2–4) (general abbreviation H2L), in the presence of vanillin (Hvan) in equimolar ratio under aerobic conditions generating the mixed-ligand oxovanadium(V)
complexes of the type [VVO(L)(van)], (1)–(4) in good yield. All the complexes are diamagnetic and exhibit only ligand-to-metal charge transfer (l.m.c.t.) band near 510 nm
in addition to intra-ligand (π → π*) transition band near 330 nm in CH2Cl2 solution. 1H-n.m.r. spectra of the complexes in CDCl3 solution indicate the presence of two isomeric forms [(1A), (1B); (2A), (2B); (3A), (3B) and (4A), (4B)] in different ratios, which is explained by the interchange of the two binding sites of van− motif between its coordinated equatorial and axial positions. Complexes display two quasi-reversible one electron reduction
peaks near +0.10 V and near +0.30 V versus s.c.e. in CH2Cl2 solution which are attributed to the successive reduction of VV→ VIV and the VIV→ VIII motifs, respectively. λmax (for l.m.c.t. transition), and the two reduction potential values (E
1/2)I (average of the first step anodic and first step cathodic peak potentials) and (E
1/2)II (average of the second step anodic and second step cathodic peak potentials) of the complexes, are found to be linearly related
to the Hammett constants (σ) of the substituents in the aryloxy ring of the hydrazone ligands. λmax, (E
1/2)I and (E
1/2)II values show large dependence: dλmax/dσ = 37.29 nm, d(E
1/2)I/dσ = 0.21 V and d(E
1/2)II/dσ = 0.21 V, respectively, on σ. 相似文献