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1.
Savita Verma Deepak M. Maher Samadhan S. Nagane Bhausaheb V. Tawade Prakash P. Wadgaonkar 《Journal of polymer science. Part A, Polymer chemistry》2019,57(5):588-597
New aromatic (co)polyesters containing pendant propargyloxy groups were synthesized by phase transfer‐catalyzed interfacial polycondensation of 5‐(propargyloxy)isophthaloyl chloride (P‐IPC) and various compositions of P‐IPC and isophthaloyl chloride with bisphenol A. FTIR and NMR spectroscopic data, respectively, revealed successful incorporation of pendant propargyloxy groups into (co)polyesters and formation of (co)polyesters with desired compositions. (Co)polyesters exhibited good solubility in common organic solvents such as chloroform, dichloromethane, and tetrahydrofuran and could be cast into transparent, flexible, and tough films from chloroform solution. Inherent viscosities and number average molecular weights of (co)polyesters were in the range 0.77–1.33 dL/g and 43,600–118,000 g/mol, respectively, indicating the achievement of reasonably high‐molecular weights. The 10% weight loss temperatures of (co)polyesters were in the range 390–420 °C, demonstrating their good thermal stability. (Co)polyesters exhibited Tg in the range 146–170 °C and Tg values decreased with increase in mol % incorporation of P‐IPC. The study of non‐isothermal curing by DSC indicated thermal crosslinking of (co)polyesters via propargyloxy groups. The utility of pendant propargyloxy group was demonstrated by post‐modification of the selected copolyester with 1‐(4‐azidobutyl)pyrene, 9‐(azidomethyl)anthracene, and azido‐terminated poly(ethyleneglycol) monomethyl ether via copper(I)‐catalyzed Huisgen 1,3‐dipolar cycloaddition reaction. FTIR and 1H NMR spectra confirmed that click reaction was quantitative. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 588–597 相似文献
2.
P. V. Badadhe N. M. Chavan D. S. Ghotekar P. G. Mandhane R. S. Joshi C. H. Gill 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):2021-2032
Abstract Synthesis of some new functionalized thiazolidin-4-ones and α-amino phosphonate derivatives has been reported. The imines were synthesized from the reaction of various substituted anilines with 1-phenyl-3-(pyridine-4-yl)-1H-pyrazole-4-carbaldehyde in ethanol at reflux condition. The corresponding thiazolidin-4-ones and α-aminophosphonates were prepared by reaction of imines with mercaptoacetic acid and triethyl phosphite, respectively. The structures of the newly synthesized compounds were confirmed by IR, 1H NMR, and mass spectral data and were evaluated for their antimicrobial activities. GRAPHICAL ABSTRACT 相似文献
3.
Abeer F. Shunnar Dr. Bhausaheb Dhokale Dr. Durga Prasad Karothu David H. Bowskill Dr. Isaac J. Sugden Dr. Hector H. Hernandez Prof. Panče Naumov Dr. Sharmarke Mohamed 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(21):4752-4765
The discovery of molecular ionic cocrystals (ICCs) of active pharmaceutical ingredients (APIs) widens the opportunities for optimizing the physicochemical properties of APIs whilst facilitating the delivery of multiple therapeutic agents. However, ICCs are often observed serendipitously in crystallization screens and the factors dictating their crystallization are poorly understood. We demonstrate here that mechanochemical ball milling is a versatile technique for the reproducible synthesis of ternary molecular ICCs in less than 30 min of grinding with or without solvent. Computational crystal structure prediction (CSP) calculations have been performed on ternary molecular ICCs for the first time and the observed crystal structures of all the ICCs were correctly predicted. Periodic dispersion-corrected DFT calculations revealed that all the ICCs are thermodynamically stable (mean stabilization energy=−2 kJ mol−1) relative to the crystallization of a physical mixture of the binary salt and acid. The results suggest that a combined mechanosynthesis and CSP approach could be used to target the synthesis of higher-order molecular ICCs with functional properties. 相似文献
4.
Tarun Kumar Chakra Tarakanta Nayak Kedarnath Senapati 《Proceedings Mathematical Sciences》2018,128(5):64
The dynamics of functions \(f_\lambda (z)= \lambda \frac{\mathrm{e}^{z}}{z+1}\ \text{ for }\ z\in \mathbb {C}, \lambda >0\) is studied showing that there exists \(\lambda ^* > 0\) such that the Julia set of \(f_\lambda \) is disconnected for \(0< \lambda < \lambda ^*\) whereas it is the whole Riemann sphere for \(\lambda > \lambda ^*\). Further, for \(0< \lambda < \lambda ^*\), the Julia set is a disjoint union of two topologically and dynamically distinct completely invariant subsets, one of which is totally disconnected. The union of the escaping set and the backward orbit of \(\infty \) is shown to be disconnected for \(0<\lambda < \lambda ^*\) whereas it is connected for \(\lambda > \lambda ^*\). For complex \(\lambda \), it is proved that either all multiply connected Fatou components ultimately land on an attracting or parabolic domain containing the omitted value of the function or the Julia set is connected. In the latter case, the Fatou set can be empty or consists of Siegel disks. All these possibilities are shown to occur for suitable parameters. Meromorphic functions \(E_n(z) =\mathrm{e}^{z}(1+z+\frac{z^2}{2!}+\cdots +\frac{z^n}{n!})^{-1}\), which we call exponential-like, are studied as a generalization of \(f(z)=\frac{\mathrm{e}^{z}}{z+1}\) which is nothing but \(E_1(z)\). This name is justified by showing that \(E_n\) has an omitted value 0 and there are no other finite singular value. In fact, it is shown that there is only one singularity over 0 as well as over \(\infty \) and both are direct. Non-existence of Herman rings are proved for \(\lambda E_n \). 相似文献
5.
Kiran S. Hon Hemantkumar N. Akolkar Bhausaheb K. Karale 《Journal of heterocyclic chemistry》2019,56(6):1780-1786
A series of novel 1‐methyl‐3‐(4‐phenyl‐4H‐1,2,4‐triazol‐3‐yl)‐1H‐indazoles was synthesized in three steps from 5‐(1‐methyl‐1H‐indazol‐3‐yl)‐4‐phenyl‐2H‐1,2,4‐triazole‐3(4H)‐thiones. 5‐(1‐Methyl‐1H‐indazol‐3‐yl)‐4‐phenyl‐2H‐1,2,4‐triazole‐3(4H)‐thiones were converted into 1‐methyl‐3‐(5‐(methylsulfonyl)‐4‐phenyl‐4H‐1,2,4‐triazol‐3‐yl)‐1H‐indazoles upon methylation followed by treatment with aq. KMnO4. The reaction of 1‐methyl‐3‐(5‐(methylsulfonyl)‐4‐phenyl‐4H‐1,2,4‐triazol‐3‐yl)‐1H‐indazoles with Raney nickel resulted in desulphonylation to afford corresponding 1‐methyl‐3‐(4‐phenyl‐4H‐1,2,4‐triazol‐3‐yl)‐1H‐indazoles. All the new synthesized compounds were characterized by spectral techniques. 相似文献
6.
Nisha Kushwah Soumyaditya Mula Amey P. Wadawale Meenakshi Joshi Kedarnath Gotluru Mukesh Kumar Tapan K. Ghanty Sandip K. Nayak Vimal K. Jain 《Journal of heterocyclic chemistry》2019,56(9):2499-2507
Salicylaldimine Schiff bases represent an important class of hetero‐polydentate ligands capable of forming mononuclear, binuclear, and polynuclear complexes with transition and non‐transition metals. In this report, we developed an easy synthesis of BODIPY‐based salicylaldimine Schiff bases and synthesized five new derivatives. These were characterized by elemental analysis, infrared, UV‐Vis, nuclear magnetic resonance spectroscopy, and X‐ray crystallography. Finally, one of the Schiff bases was reacted with BF3·OEt2 to synthesize corresponding bis‐BF2 boron complex. The photophysical and electrochemical properties of the Schiff bases and the boron complex were evaluated and rationalized by theoretical calculations. The bis‐BF2 boron complex showed excited state charge redistribution, thus could be useful as sensitizers for designing new dye‐sensitized solar cells. 相似文献
7.
Rahul D. Shingte Deepshikha Chatterjee Bhausaheb V. Tawade Bharat Shrimant 《高分子科学杂志,A辑:纯化学与应用化学》2019,56(2):136-145
Three bisphenols containing cardo perhydrocumyl cyclohexylidene group, namely; 1,1-bis(4-hydroxyphenyl)-4-perhydrocumylcyclohexane, 1,1-bis(4-hydroxy-3-methylphenyl)-4-perhydrocumylcyclohexane and 1,1-bis(4-hydroxy-3,5-dimethylphenyl)-4-perhydrocumylcyclohexane were synthesized starting from p-cumyl phenol. Each of these bisphenols was polycondensed with both terephthaloyl chloride and isophthaloyl chloride by phase transfer-catalyzed interfacial polymerization to obtain a series of new aromatic polyesters. Inherent viscosities and number average molecular weights of polyesters were in the range 0.51-0.64 dL/g and 17390-41430?g/mol, respectively which indicated the formation of reasonably high molecular weight polymers. The detailed NMR studies revealed that axial and equatorial identity of the phenyl rings of bisphenols was retained in polyesters resulting in constitutional isomerism. Polyesters containing perhydrocumyl cyclohexylidene groups showed excellent solubility in organic solvents viz, chloroform, dichloromethane, 1,1,2,2-tetrachloroethane and tetrahydrofuran. The self-standing films of polyesters could be cast from their chloroform solution. The 10% weight loss temperatures and glass transition temperatures of polyesters were in the range 453–485?°C and 201–267?°C, respectively demonstrating their excellent thermal characteristics. The gas permeability study of polyesters was carried out for He, H2 and N2 by variable-volume method. An improvement in permeability and decrease in selectivity was observed due to symmetric methyl substituents while reverse trend was observed in case of polyesters with asymmetric methyl substituents. 相似文献
8.
Raghunath B. Toche Bhausaheb K. Ghotekar Dhananjay B. Kendre Muddassar A. Kazi Madhukar N. Jachak 《Journal of heterocyclic chemistry》2008,45(6):1711-1717
5‐Chloroethylpyrazolo[3,4‐b]pyridines were synthesized by condensation of 5‐aminopyrazoles with α‐acetyl γ‐butyrolactone followed by cyclization treating with phosphorous oxychloride. 5‐Chloroethyl‐pyrazolo[3,4‐b]pyridines, thus obtained, were then converted to the corresponded tricyclic pyrazolo[3,4‐b]‐pyrrolo[2,3‐d]pyridines by treating with some primary amines. 相似文献
9.
Madhukar N. Jachak Sandeep M. Bagul Bhausaheb K. Ghotekar Raghunath B. Toche 《Monatshefte für Chemie / Chemical Monthly》2009,140(6):655-662
Abstract A series of (2E)-3-(1-chloro-6-methoxy-3,4-dihydronaphthalen-2-yl)-1-(4-aryl)prop-2-en-1-ones (chalcones) have been synthesized by a new
synthetic route. The 3-pyridinecarbonitrile derivatives were synthesized by the Michael reaction of malononitrile (in base)
and aroylacetonitriles (in acid) with chalcones in one pot. The fluorescent properties and quantum yields of these compounds
were studied.
Graphical Abstract
相似文献
10.
Madhukar N. Jachak Sandeep M. Bagul Bhausaheb K. Ghotekar Raghunath B. Toche 《Monatshefte für Chemie / Chemical Monthly》2009,20(5):655-662