- 标题
- 摘要
- 关键词
- 实验方案
- 产品
-
Effect of Unsymmetrically Branched Alkyl Chains on the Electrochemical Band Gap and Thermal Stability of the PCDTBT
摘要： This work introduces a modified poly[N-9’-heptadecanyl-2,7-carbazole-alt-5,5-(4’,7’-di-2-thienyl-2’,1’,3’-benzothiadiazole)] (PCDTBT) with the unsymmetrically branched N-alkyl chain, which name as poly[N-9’-(2-hexyldecyl)-2,7-carbazole-alt-5,5-(4’,7’-di-2-thienyl-2’,1’,3’-benzothiadiazole)] (P1). The synthesis of P1 involves dimerization, cyclization, tosylation, N-alkylation, bromination, Stille’s and Suzuki’s coupling reactions. Suitable analysis techniques have used to study the chemical, physical, electrochemical, optical, and thermal properties of P1. The analysis results show that P1 possesses higher HOMO and LUMO energy levels than the previously reported PCDTBT, which have been narrowing the electrochemical band gap down to 1.58 eV. However, the P1 experiences 5% thermal degradation at 280 °C, which is relatively less favourable than the PCDTBT. Hence, the replacement of the symmetrically branched alkyl chains of PCDTBT with unsymmetrically branched alkyl chains results in both improvement and draw-back on the characteristics of the polymer.
关键词： bond energy,Alkylation,cyclic voltammetry,electrochemistry,polymerization
更新于2025-11-19 16:56:35
-
Competing photochemical reactions of bis-naphthols and their photoinduced antiproliferative activity
摘要： Photophysical properties and photochemical reactivity for a series of bis-naphthols 4a-4e and bis-anthrols 5a and 5e were investigated by preparative irradiations in CH3OH, fluorescence spectroscopy and laser flash photolysis (LFP). Methanolysis taking place via photodehydration (bis-naphthols ΦR = 0.04-0.05) is in competition with symmetry breaking charge separation (SB-CS). The SB-CS gives rise to radical ions that were for 4a and 4e detected by LFP. Photodehydration gives quinone methides (QMs) that were also detected by LFP (λmax = 350 nm, τ ≈ 1-2 ms). In the aqueous solvent, excited state proton transfer (ESPT) competes with the above mentioned processes, giving rise to naphtholates, but the process is inefficient and can only be observed in the buffered aqueous solution at pH >7. Since the dehydration of bis-naphthols delivers QMs, their potential antiproliferative activity was investigated by MTT test on three human cancer cell lines (NCI-H1299, lung carcinoma; MCF-7, breast adenocarcinoma; and SUM159, pleomorphic breast carcinoma). Cells were treated with 4 or 5 with or without irradiation (350 nm). An enhancement of the activity (up to 10-fold) was observed upon irradiation, which may be associated to the QM formation. However, these QMs do not cross-link DNA. The activity is most likely associated to the alkylation of proteins present in the cell cytoplasm, as evidenced by photoinduced alkylation of bovine and human serum albumins by 4a.
关键词： quinone methides,bis-anthrols,excited state proton transfer,protein alkylation,bis-naphthols,antiproliferative activity,photodehydration,symmetry breaking charge separation
更新于2025-11-14 15:32:45
-
Study of the Synthetic Potential of the Reaction of Benzimidazole with Bis(iodomethyl)tetramethyldisiloxane by Matrix-Free Laser Desorption/Ionization Mass Spectrometry
摘要： According to the matrix-free laser desorption/ionization time-of-flight mass spectrometric data, the reaction of benzimidazole with bis(iodomethyl)tetramethyldisiloxane at different temperatures leads to the formation of linear and cyclic organosilicon systems containing benzimidazole fragments. The structures of the major and minor products were determined by analysis of the fragmentation patterns in the field-free space.
关键词： bis(iodomethyl)tetramethyldisiloxane,benzimidazole,insertion,fragmentation,alkylation,silanone,laser desorption/ionization
更新于2025-09-23 15:21:01
-
Enantioselective Allylic Alkylation with 4-Alkyl-1,4-dihydropyridines Enabled by Photoredox/Palladium Cocatalysis
摘要： Highly regio-, and enantioselective allylic alkylation has been achieved enabled by the merger of photoredox and palladium catalysis. In this dual catalytic process, alkyl radicals generated from 4-alkyl-1,4-dihydropyridines act as the coupling partners of the π-allyl palladium complexes. The generality of this method has been illustrated through the reaction of a variety of allyl esters with 4-alkyl-1,4-dihydropyridines. This mechanistically novel strategy expands the scope of the traditional Pd-catalyzed asymmetric allylic alkylation reaction and serves as its alternative and potential complement.
关键词： π-Allyl Palladium Complexes,Palladium Catalysis,4-Alkyl-1,4-dihydropyridines,Photoredox Catalysis,Enantioselective Allylic Alkylation
更新于2025-09-09 09:28:46