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61.
Partially bio‐based poly(amide imide)s by polycondensation of aromatic diacylhydrazides based on lignin‐derived phenolic acids and aromatic dianhydrides: Synthesis,characterization, and computational studies 下载免费PDF全文
Sachin S. Kuhire Pragati Sharma Suman Chakrabarty Prakash P. Wadgaonkar 《Journal of polymer science. Part A, Polymer chemistry》2017,55(21):3636-3645
Two new bio‐based diacylhydrazide monomers, namely, 4,4′‐(propane‐1,3‐diylbis(oxy))bis(3‐methoxybenzohydrazide) and 4,4′‐(propane‐1,3‐diylbis(oxy))bis(3,5‐dimethoxybenzohydrazide) were synthesized starting from lignin‐derived phenolic acids, namely, vanillic acid and syringic acid. A series of poly(amide imide)s was synthesized by polycondensation of these diacylhydrazide monomers with commercially available aromatic dianhydrides. Poly(amide imide)s showed inherent viscosity in the range 0.44–0.56 dL g?1 and exhibited good solubility in organic solvents. Poly(amide imide)s could be cast into transparent, flexible, and tough films from their N ,N‐dimethylacetamide solutions. Poly(amide imide)s showed 10% weight loss in the temperature range 340–364 °C indicating their good thermal stability. Glass transition temperature (T g) of poly(amide imides)s were measured by DSC and DMA which were in the range 201–223 °C and 214–248 °C, respectively. The T g values of poly(amide imide)s were dependent on the number methoxy substituents on aromatic rings of diacylhydrazide monomers. Molecular dynamics simulation studies revealed that chain rigidity is the dominant factor for observed trends in T g. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 3636–3645 相似文献
62.
50% Ethanolic or aqueous formic acid has been found to be extremely efficacious for the regeneration of aliphatic and aromatic ketones from phenylhydrazones. 相似文献
63.
64.
Haldar B Chakrabarty A Mallick A Mandal MC Das P Chattopadhyay N 《Langmuir : the ACS journal of surfaces and colloids》2006,22(8):3514-3520
Steady-state fluorescence measurements and isothermal titration calorimetric experiments have been performed to study the interaction between a telechelic polymer, pyrene-end-capped poly(ethylene oxide) (PYPY), and sodium alkyl sulfate surfactants having decyl, dodecyl, and tetradecyl hydrocarbon tails. Fluorometric results suggest polymer-surfactant interaction in the very low range of polymer concentrations. The relative variation in the excimer to monomer pyrene emission intensities with varying surfactant concentration reveals that initial addition of surfactant favors intramolecular preassociation until the surfactant molecules start binding with the ethylene oxide (EO) chain. With the growing number of surfactant aggregates along the EO chain, the association becomes hindered due to the polyelectrolyte effect. The results from microcalorimetric titrations in the low concentration range of PYPY solution (approximately 10(-6) M) with alkyl sulfates suggest two kinds of surfactant-polymer interactions, one with the polymer hydrophobic end groups and the other with the ethylene oxide backbone. The overall polymer-surfactant interaction starts at a much lower surfactant concentration for the hydrophobically modified polymers compared to that in the case of unsubstituted poly(ethylene oxide) homopolymer. From the experiments critical aggregation concentration values and the second critical concentration where free micelles start forming have been determined. An endeavor has been made to unveil the mechanism underlying the corresponding associations of the surfactants with the polymer. 相似文献
65.
Das P Mallick A Chakrabarty A Haldar B Chattopadhyay N 《The Journal of chemical physics》2006,125(4):44516
In continuation of our recent study on the steady state photophysics of a biologically active beta-carboline derivative, 3-acetyl-4-oxo-6,7-dihydro-12H indolo-[2,3-a] quinolizine (AODIQ), in the present article we have investigated the effect of nanocavity confinement on the excited state dynamics and rotational relaxation of the probe using picosecond time resolved fluorescence and fluorescence anisotropy techniques. The polarity dependent intramolecular charge transfer process is responsible for the remarkable sensitivity of this biological fluorophore in micellar environments. The fluorescence anisotropy decay of AODIQ incorporated inside the micelle is biexponential. The rotational motion of the probe was interpreted on the basis of a two step model consisting of a fast restricted rotation of the probe and a slow lateral diffusion of the probe in the micelle; both coupled to the overall rotation of the micelle. Experimental results reveal that micellar environment causes significant retardation of both the wobbling as well as the translational motion of the probe. 相似文献
66.
Chakrabarty D Chakraborty A Seth D Sarkar N 《The journal of physical chemistry. A》2005,109(9):1764-1769
The dynamics of solvent relaxation in ionic liquid (IL)-water, IL-methanol, and IL-acetonitrile mixtures have been investigated using steady state and picosecond time-resolved fluorescence spectroscopy. We have used Coumarin 153 (C-153) and 1-hexyl-3-methylimidazolium hexafluorophosphate ([hmim][PF(6)]) as fluorescence probe and IL, respectively. The steady-state emission spectra showed that the gradual addition of cosolvents increases the polarity of the mixtures. In neat [hmim][PF(6)] and all IL-cosolvent mixtures, solvation occurs in two well-separated time regimes within the time resolution of our instrument. A substantial portion of the solvation has been missed due to the limited time resolution of our instrument. The gradual addition of cosolvents decreases the viscosity of the medium and consequently solvation time also decreases. The decrease in solvation time is more pronounced on addition of acetonitrile compared to water and methanol. The rotational relaxation time of the probe is also decreasing with gradual addition of the cosolvents. The decrease in viscosity of the solution is responsible for the decrease in the rotational relaxation time of the probe molecule. 相似文献
67.
A method for quantitative extraction of zinc with potassium ethyl xanthate into carbon tetrachloride is described. The optimum conditions are: pH 5-6 and Zn(II) to reagent ~1:8 mole ratio. The effects of other ions on the extraction of Zn(2+) have been investigated, and its separation from As(3+), Pb(2+), Cu(2+) and Fe(3+)is described. The possibility of repeated use of the solvent (still loaded with xanthate after the zinc has been stripped) for further extractions (after addition of a little extra xanthate) has been explored. Various stripping agents have been examined, and the optimum conditions found. 相似文献
68.
69.
S. Chakrabarty 《Fortschritte der Physik》1991,39(3):159-184
In this article we give a review of certain aspects of the present understanding of spectroscopy of heavy mesons and constituent quark masses in the light of non-relativistic potential model approach motivated by quantum chromodynamics. We find that the one gluon exchange at short distance and colour-confining interaction at large distance which is pure scalar (or scalarvector admixture with dominant scalar interaction) under the Lorentz transformation, can explain only partially the present data on 1 P states of bb and bb states. The S-wave data, that are available at present, however can be understood with both scalar confinement or scalar-vector admixture with scalar-dominant interaction. 相似文献
70.
D. P. Bhattacharyya S. Chakrabarty R. Rakshit B. Basu Pratibha Pal S. Biswas 《Il Nuovo Cimento C》1993,16(3):249-254
Summary A stack consisting of CR-39(DOP) detector with 2.6 cm Al target was exposed to a238U beam of energy 0.927 GeV/n from LBL BEVALAC to study the large-fragmentation phenomena during U+Al interaction. The diameter
distribution of the etch pits formed in the plastic detectors for the first three projectile fragments of chargeZ
F≥89 yields the partial cross-section data which is comparable to the data obtained from the cone length distribution. The
present result on the partial cross-section is significantly higher than those expected from the abrasion-ablation model of
Wilson, Townsed and Badavi (1987).
The authors of this paper have agreed not to receive the proofs for correction. 相似文献