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1.
Vishal Kandathil Aisha Siddiqa Abhinandan Patra Bhakti Kulkarni Manjunatha Kempasiddaiah B.S. Sasidhar Shivaputra A. Patil Chandra Sekhar Rout Siddappa A. Patil 《应用有机金属化学》2020,34(11):e5924
N-heterocyclic carbene (NHC)-palladium(II) complex (GO@NHC-Pd) was synthesized on graphene oxide (GO) support via a simple and cost-effective multistep approach. The spectroscopic, microscopic, thermal, and surface analyses of GO@NHC-Pd confirmed the successful formation of the catalyst. The investigation of catalytic activity showed that GO@NHC-Pd was very effective in Suzuki–Miyaura as well as Hiyama cross-coupling. Being heterogeneous in nature, GO@NHC-Pd was recovered after each reaction cycle easily and reused for up to nine and six cycles in Suzuki–Miyaura and Hiyama cross-coupling, respectively, without significant loss of activity. Further exploration of the supercapacitor performance of GO@NHC-Pd catalyst assembled in a two-electrode cell configuration shown a maximum attained capacitance of 105.26 F/g at a current density of 0.1 A/g with good cycling stability of 96.89% over 2,500 cycles. 相似文献
2.
Rahul S. Patil Dr. Debasis Banerjee Cory M. Simon Prof. Jerry L. Atwood Dr. Praveen K. Thallapally 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(36):12618-12623
Separation of xenon and krypton is of industrial and environmental concern; the existing technologies use cryogenic distillation. Thus, a cost‐effective, alternative technology for the separation of Xe and Kr and their capture from air is of significant importance. Herein, we report the selective Xe uptake in a crystalline porous organic oligomeric molecule, noria, and its structural analogue, PgC‐noria, under ambient conditions. The selectivity of noria towards Xe arises from its tailored pore size and small cavities, which allows a directed non‐bonding interaction of Xe atoms with a large number of carbon atoms of the noria molecular wheel in a confined space. 相似文献
3.
Gold(I)/Chiral Brønsted Acid Catalyzed Enantioselective Hydroamination–Hydroarylation of Alkynes: The Effect of a Remote Hydroxyl Group on the Reactivity and Enantioselectivity 下载免费PDF全文
Valmik S. Shinde Manoj V. Mane Dr. Kumar Vanka Arijit Mallick Dr. Nitin T. Patil 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(3):975-979
The catalytic enantioselective hydroamination–hydroarylation of alkynes under the catalysis of (R3P)AuMe/(S)‐3,3′‐bis(2,4,6‐triisopropylphenyl)‐1,1′‐binaphthyl‐2,2′‐diyl hydrogenphosphate ((S)‐TRIP) is reported. The alkyne was reacted with a range of pyrrole‐based aromatic amines to give pyrrole‐embedded aza‐heterocyclic scaffolds bearing a quaternary carbon center. The presence of a hydroxyl group in the alkyne tether turned out to be very crucial for obtaining products in high yields and enantioselectivities. The mechanism of enantioinduction was established by carefully performing experimental and computational studies. 相似文献
4.
Rane Vipul P. Patil Rushikesh H. Patil Kiran R. Pathan Amin R. Naik Sukantakumar Ahirrao Vinod K. Jadhav Rajiv A. Yeole Ravindra D. 《Chromatographia》2022,85(2):155-165
Chromatographia - WCK 771 is a novel antibacterial drug recently launched in India for the treatment of acute bacterial skin and skin structure infections (ABSSSI). This report describes... 相似文献
5.
Kiran Patil Amin Pathan Sukanta Naik Vineet Zope Rajesh Chavan Ravindra Yeole 《Biomedical chromatography : BMC》2022,36(7):e5377
A precise and accurate liquid chromatography–tandem mass spectrometric (LC–MS/MS) bioanalytical method has been developed and validated for the simultaneous quantification of WCK 4234 and meropenem (MEM) in dog plasma. Protein precipitation using acetonitrile was employed as a sample preparation approach. Cefepime was used as an internal standard. The developed method was selective, sensitive (limit of quantification, 0.075 μg/ml for both drugs), accurate (recovery > 90%), precise (CV < 10%) and linear (r2 ≥ 0.99, concentration range 0.075–120 μg/ml for both analytes). The developed method was successfully applied for the determination of both drugs in plasma to assess the pharmacokinetics in beagle dogs. WCK 4234 + MEM in a 1:1 ratio at 15 + 15 and 30 + 30 mg/kg doses were administered by the intravenous route. The mean plasma concentration and area under the concentration–time curve of WCK 4234 ranged from 38.3 to 77.4 μg/ml and from 47.8 to 77.1 μg h/ml, respectively, and the values for MEM ranged from 52.2 to 115.3 μg/ml and 70.5 to 133.6 μg h/ml respectively. The elimination half-life of WCK 4234 and MEM was around 0.8 h. 相似文献
6.
Yogesh Patil George Zapsas Yves Gnanou Nikos Hadjichristidis 《Journal of polymer science. Part A, Polymer chemistry》2020,58(1):163-171
This study presents the synthesis and properties of linear PVDF-based amphiphilic triblock terpolymers with PS and PEO, [PVDF-b-PS-b-PEO], by adopting a procedure that involves: (a) iodine-transfer polymerization (ITP) of VDF with 1-iodoperfluorohexane (C6F13I) serving as chain-transfer agent (CTA) to afford C6F13-PVDF-I, (b) ITP of styrene with the C6F13-PVDF-I macromolecular-CTA to obtain C6F13-PVDF-b-PS-I diblock copolymer, (c) end-group exchange from iodo- to azido-group by nucleophilic substitution reaction with NaN3, and (d) copper-catalyzed azide-alkyne cycloaddition (CuAAC) with alkyne-terminated PEO to achieve C6F13-PVDF-b-PS-b-PEO triblock terpolymers. The 1H and 19F NMR spectroscopy confirmed the presence of all blocks, while gel permeation chromatography traces showed the living nature of ITP technique. The self-assembly of these terpolymers was investigated in films (atomic force microscopy and DSC), as well as in aqueous and organic solvents (DLS). The analysis of crystalline phases based on the FTIR spectroscopy indicated the conversion of PVDF α-phase into α + β-phases and β + γ-phases upon the incorporation of PS and PEO blocks, respectively. The synthesized amphiphilic copolymers were evaluated (fluorescence spectroscopy) as carriers of small hydrophobic molecules in water. © 2019 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 163–171 相似文献
7.
Vivek W. Bhoyare Akash G. Tathe Prof. Vincent Gandon Dr. Nitin T. Patil 《Angewandte Chemie (International ed. in English)》2023,62(46):e202312786
The successful realization of gold-catalyzed chain-walking reactions, facilitated by ligand-enabled Au(I)/Au(III) redox catalysis, has been reported for the first time. This breakthrough has led to the development of gold-catalyzed annulation reaction of alkenes with iodoarenes by leveraging the interplay of chain-walking and π-activation reactivity mode. The reaction mechanism has been elucidated through comprehensive experimental and computational studies. 相似文献
8.
Interfacial Engineering of CdO–CdSe 3D Microarchitectures with in situ Photopolymerized PEDOT for an Enhanced Photovoltaic Performance 下载免费PDF全文
Iseul Lim Dipak V. Shinde Supriya A. Patil Do Young Ahn Wonjoo Lee Nabeen K. Shrestha Joong Kee Lee Sung‐Hwan Han 《Photochemistry and photobiology》2015,91(4):780-785
In the present work, porous 3D CdO‐microstructured electrode obtained by pyrolysis of 3D CdCO3 microstructures is self‐sensitized with CdSe using an ion exchange reaction. After sensitization, an interfacial treatment of the CdO–CdSe interface is performed by depositing a thin film of PEDOT using a photoinduce polymerization route. The microstructured electrode before and after interfacial treatment is characterized using field‐emission scanning microscope, energy dispersive X‐ray analyzer, contact angle measurement, UV–Visible absorption spectrophotometer and X‐ray photoelectron spectrometer. After constructing a liquid junction solar cell with a Pt counter electrode, the photovoltaic performance and interfacial charge transfer kinetics across the CdO–CdSe interface before and after PEDOT treatment are investigated. The results exhibit an improved interfacial charge‐transfer resistance after the PEDOT treatment, which leads to enhance the short‐circuit current by 15.81% and the power conversion efficiency by 19.82%. 相似文献
9.
Synthesis,Characterization, and Antibacterial Activity of Novel (1H‐Benzo[d]imidazole‐2‐yl)‐6‐(diethylamino)‐3H‐one‐xanthene,Phenoxazine, and Oxazine 下载免费PDF全文
Vikas S. Patil Vikas S. Padalkar Kiran R. Phatangare Prashant G. Umape Bhushan N. Borase N. Sekar 《Journal of heterocyclic chemistry》2015,52(1):124-129
A series of novel (1H‐benzo[d]imidazole‐2‐yl)‐6‐(diethylamino)‐3H‐one‐xanthene, phenoxazine, and oxazine derivatives have been synthesized from 2‐(2′,4′‐dihydroxyphenyl) benzimidazole intermediate. Synthesized compounds 8a , 8b , 8c , 8d are fluorescent in solution, photophysical properties of compounds were studied and results revealed that compounds absorb and emit in UV–visible region with good fluorescence quantum yield. Synthesized compounds are thermally stable up to 300°C. The antibacterial activities of the synthesized compounds were studied by the well‐diffusion method. Escherichia coli (ATTC‐25922), Staphylococcus aureus (ATCC‐25923), Micrococcus (ATCC‐4698), and Bacillus subtilis (ATCC‐55422) were used to investigate the antibacterial activities. 相似文献
10.