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1.
Janina Kabatc Małgorzata Gruszewska Beata Jędrzejewska Jerzy Pączkowski 《Polymer Bulletin》2007,58(4):691-701
Summary The series of 6-bromo-3-ethyl-2-styrylbenzothiazolium n-butyltriphenylborates was synthesized and evaluated as photoinitiators of free radical polymerization. The dyes were obtained
by the condensation reaction of the 6-bromo-3-ethyl-2-methylbenzothiazolium salts with different alkylaminobenzaldehydes.
The resulting styrylbenzothiazole dyes (hemicyanine dyes) paired with n-butyltriphenylborate anion (SBrB2), are shown to be efficient photoinitiators for free radical polymerization of trimethylolpropane triacrylate (TMPTA) induced
with the visible emission of an argon-ion laser. The photochemistry of the novel hemicyanine borates was compared to the photochemistry
of identical series of the dyes that do not possess the bromo substituent at benzothiazolium residue. The comparison has shown
that the introduction of the bromine into benzothiazolium residue causes a small red shift of the electronic absorption maxima,
changes the reduction potential of the dye and, finally, increases a photoinitiation ability of the dye. 相似文献
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Dr. Mohit Chawla Dr. Yury Minenkov Prof. Dr. Khanh B. Vu Prof. Dr. Romina Oliva Prof. Dr. Luigi Cavallo 《Chembiochem : a European journal of chemical biology》2019,20(17):2262-2270
The impact of 7-deaza-8-azaguanine (DAG) and 7-deaza-8-azaisoguanine (DAiG) modifications on the geometry and stability of the G:C Watson–Crick (cWW) base pair and the G:iC and iG:C reverse Watson–Crick (tWW) base pairs has been characterized theoretically. In addition, the effect on the same base pairs of seven C7-substituted DAG and DAiG derivatives, some of which have been previously experimentally characterized, has been investigated. Calculations indicate that all of these modifications have a negligible impact on the geometry of the above base pairs, and that modification of the heterocycle skeleton has a small impact on the base-pair interaction energies. Instead, base-pair interaction energies are dependent on the nature of the C7 substituent. For the 7-substituted DAG-C cWW systems, a linear correlation between the base-pair interaction energy and the Hammett constant of the 7-substituent is found, with higher interaction energies corresponding to more electron-withdrawing substituents. Therefore, the explored modifications are expected to be accommodated in both parallel and antiparallel nucleic acid duplexes without perturbing their geometry, while the strength of a base pair (and duplex) featuring a DAG modification can, in principle, be tuned by incorporating different substituents at the C7 position. 相似文献
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Hikishima S Minakawa N Kuramoto K Ogata S Matsuda A 《Chembiochem : a European journal of chemical biology》2006,7(12):1970-1975
We describe the synthesis and properties of oligodeoxynucleotides (ODNs) containing 1,8-naphthyridine C-nucleoside (Na-NO) and imidazo[5',4':4,5]pyrido[2,3-d]pyrimidine nucleoside (Im-ON) at the termini. The modified ODNs were more resistant (6 to 40 times) than natural DNA to snake venom phosphodiesterase (SVPD). Although incorporation of one pair each of Na-NO:Im-ON on the sticky ends of the duplex was insufficient for thermal stabilization (+2.5 degrees C per pair relative to the G:C pair), the duplex containing two consecutive Na-NO:Im-ON pairs at its sticky ends was markedly stabilized thermally. The stabilizing effect of the incorporation of additional Na-NO:Im-ON pairs is estimated to be +7.8 degrees C per pair. Application as thermally stabilized decoy molecules to NF-kappaB (p50) was also demonstrated. The DNA duplexes containing the Na-NO:Im-ON pairs (ODN I:ODN II and ODN III:ODN IV) acted as competitors to the natural NF-kappaB-binding duplex (ODN V: ODN VI), and the calculated IC50 values of ODN I:ODN II and ODN III:ODN IV were 20.1+/-13.3 and 10.9+/-4.8 nM, respectively, greater than that of ODN V:ODN VI. 相似文献
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Bromo‐based and acetated‐based ionic liquids (ILs), 1‐butyle‐3‐methylimidazolium bromo ([Bmim]Br), 1‐ethyl‐3‐mthylimidazolium bromo ([Emim]Br), 1‐butyle‐3‐methylimidazolium acetate ([Bmim]Ac), and 1‐ethyl‐3‐mthylimidazolium acetate ([Emim]Ac), were synthesized and employed for wool surface treatment. Scanning electron microscope results indicated that the wool surfaces treated with acetated‐based ILs were eroded more than those treated with bromo‐based ILs. Comparable studies showed that the wool samples treated with acetate‐based ILs, especially [Emim]Ac, had higher initial dyeing rate and equilibrium exhaustion than those with bromo‐based ILs. Along with treatment temperature and time increasing, acetate‐based ILs had more remarkable effects on mechanical and dyeing properties of the wool samples than bromo‐based ILs. The wool samples treated with [Emim]Ac at 60°C for 10 min had excellent low‐temperature dyeing properties. The color depth (K/S) investigations showed that the wool samples treated with acetate‐based ILs possessed darker color depth than those treated with the bromo‐based ILs. Color fastnesses of the wool samples treated with [Bmim]Br, [Emim]Br and [Bmim]Ac exhibited the same grades as the untreated sample, while wet color fastnesses of [Emim]Ac treated sample were slightly decreased. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 相似文献
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Synthesis and Electron Paramagnetic Resonance Studies of Oligodeoxynucleotides Containing 2‐N‐tert‐Butylaminoxyl‐2′‐deoxyadenosines
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Manami Kurita Yoshitaka Higuchi JW Mirc Shintaro Matsumoto Dr. Kazuteru Usui Prof. Dr. Hiroshi Suemune Dr. Mariko Aso 《Chembiochem : a European journal of chemical biology》2016,17(24):2346-2352
Oligodeoxynucleotides (ODNs) containing 2‐N‐tert‐butylaminoxyl‐2′‐deoxyadenosine ( A* ) residues were synthesized to allow accurate monitoring of adenine motion by EPR spectroscopy through the agency of direct linkage of the acyclic aminoxyl group to the nucleobase, and EPR studies of the ODNs in single‐ and double‐stranded forms were performed. Upon duplex formation, peak broadening and decreases in peak height were observed in EPR spectra, and the synthesized ODNs were shown to be excellent monitors of hybridization. Comparison of peak height and the h1/h0 signal ratio provided information on the relative mobility of A* in duplexes with different stability. A second set of ODNs each containing two A* residues at different intervals and four dA residues were also synthesized. For these ODNs, correlations were observed between the EPR spectral shapes of the duplexes and the number of dA residues between A* residues, thus demonstrating the potential of A* residues in monitoring of the structures of nucleic acids. 相似文献
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The crystal structure of 2-bromo-4-cyano-4′-N,N-diethylaminoazobenzene has been determined from X-ray diffraction data: C17H17N4Br, mol. wt = 357·1. Triclinic, Pī (No. 2), α = 13·162(5) Å, b = 7·516(3) Å, c = 8·496(4) Å, α = 101·63(4)°, β = 95·79(4)°, γ = 91·49(4)°, V = 818·10 Å3, Z = 2, Dc = 1·45 g cm?3, F(000) = 378, λ(MoKz) = 0·7107 Å, μ(MoKα) = 26·70 cm?1. The structure was solved by direct methods and refined by full-matrix least-squares to R = 0·053 for 2081 independent reflexions. The molecule possesses an essentially planar azobenzene skeleton. The effects of substituents on the geometry of the azo group are discussed. Significant molecular parameters are: NN, 1·264(6) Å; 1BrC, 1·904(5) Å; mean NC, 1·410(7) Å; NNC, 115·7(2)° and 113·0(2)°; NCC (cis relative to NN), 125·4(3)° and 123·1(2)°; CC(Br)C, 123·0(2)°. 相似文献
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4-Bromo-3-methylanisole is mainly used to synthesize black fluorane dye(2-anilino-3-methyl-6-dibutylaminofluorane, ODB-2), which is one of the most important heat and pressure-sensitive dyes in the manufacture of thermal papers. Compared to the industrial heterogeneous batch process, a continuous homogeneous bromination technology in a modular microreaction system has been developed, and 4-bromo-3-methylanisole has been successfully prepared through high-selective mono-bromination of 3-methylanisole with Br_2 solution in CHCl_3. In optimal conditions, the content of bis-brominated byproducts can be controlled less than 0.5%,which is superior to the industrial standard with 99.5% 3-methylanisole conversion at very short residence time and mild reaction temperature. 相似文献
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1,4二-氢-3H-2,3苯-并口恶嗪-3甲-酸乙酯经过硝化、还原和重氮化溴代得到了7溴--1,4二-氢-3H-2,3苯-并口恶嗪-3甲-酸乙酯(C)。以Pd(OAc)2/R(+)B INAP(2,2′-二苯膦-1,1′-联萘)为催化体系,C与苯胺、N-甲基苯胺、对氟苯胺、对乙氧基苯胺、环己胺、吗啡、四氢吡咯及六氢吡啶等8种有机胺类化合物(Am ine1~8),在氮气保护下,以碳酸铯为碱于干燥的甲苯中100℃反应16~24 h,生成了相应的8种新的7胺-基取代的1,4二-氢-3H-2,3苯-并口恶嗪-3甲-酸乙酯类化合物(D1~8),反应收率分别为83%、85%、71%、90%、72%、63%、75%和83%。通过1HNMR、质谱和元素分析对这些化合物的结构进行了表征。 相似文献
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根据微化工技术发展的主要趋势,针对4-溴-3-甲基苯甲醚间歇非均相合成技术存在的问题,以微筛孔反应器与玻璃微珠填充床为核心功能微设备单元构建了模块化微反应系统,并在此模块化微反应系统内对液-液非均相连续溴化合成4-溴-3-甲基苯甲醚开展研究。通过优化操作条件,在溴浓度( )为17.5%(质量分数)、溴与间甲基苯甲醚摩尔比( /nM)为1.01、反应起始温度(T)为 0℃、停留时间为0.78 min条件下,4-溴-3-甲基苯甲醚的收率大于98%,多溴代副产物的含量仅为1%。与传统间歇溴化反应相比,模块化微反应系统内连续溴化反应具有十分明显的优势:可将间歇过程连续化,在保证安全的基础上极大地提升了反应的效率(时空收率为6.5×104 kg/(m3·h));另外,该过程是由传质控制的,微反应器的传质性能优异,可极大地改善产品的选择性(多溴代副产物的量减少50%)。该研究为4-溴-3-甲基苯甲醚的连续高效安全合成提供了技术和设备依据。 相似文献
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With the development of microreaction technology and the key issues of liquid-liquid batch bromination process for the synthesis of 4-bromo-3-methylanisole, a modular microreaction system was constructed by taking microreactor and microbead-packed bed as the major functional microdevice units to intensify the bromination of methylanisole. And in this modular microreaction system, the liquid-liquid heterogeneous continuous bromination of 4-bromo-3-methylanisole was studied. The following optimized conditions were obtained, concentration of Br2 (xBr2): 17.5 wt%, molar ratio of Br2 to methylanisole (nBr2/nM): 1.01, initial reaction temperature (T): 0℃, residence time (τ): 0.78 min, with yield of 4-bromo-3-methylanisole more than 98%, and percentage of polybrominated side product less than 1%. Comparing with the conventional batch process, the continuous microreaction technology has obvious advantages. For example, it can change the traditional batch process to a continuous one with a significant increase of productivity (space time yield: 6.5×104 kg/(m3·h)). Besides, since this process is mainly controlled by mass transfer, the modular microreaction system with excellent mass transfer could reduce 50% of polybrominated side product. The study might provide a good foundation for the continuously controllable synthesis of 4-bromo-3-methylanisole in safety. 相似文献
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The crystal structure and molecular conformation of 2-cyano-4-bromo-4′-N,N-diethylaminoazobenzene (C17H17N4Br, mol. wt. = 357·2 a.m.u) has been determined from X-ray diffraction data; triclinic, P (No. 2), a = 10·132(11) Å, b = 12·216(16) Å, c = 6·966(11) Å, α = 104·21(9)°, β = 92·67(12)°, γ = 97·22(7)°, V = 826·5(9) Å3, Z = 2, Dc = 1·436 g cm?3, F(000) = 378, λ(MoKα) = 0·71069 Å, μ(MoKα) = 26·0 cm?1. The structure was solved by the multiple solution direct method and refined by full-matrix least-squares to R = 0·059 for 1538 independent observed reflections. The azobenzene skeleton is planar to within 0·06 Å. Most significant bonding data are: NN, 1·290(8) Å; BrC, 1·866(6) Å; mean CN (azo) 1·380(8) Å; NNC, 113·6(4) and 115·3(4)°; NCC (cis relative to NN) 125·9(4)° and 126·7(4)°; NCC (trans) 116·8°(5)° and 116·1(4)°. 相似文献
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以邻三氟甲氧基苯胺为原料经硝化、重氮化、还原和水解四步可得纯度≥99%(GC)的产物3-溴-4-三氟甲氧基苯酚,总产率26.2%。产物结构通过MS及1H NMR验证。 相似文献
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The outer surface of multi-walled carbon nanotubes (MWCNTs) was successfully modified with 7-bromo-9,9-dioctylfluorene-2-carbaldehyde by using 1,3-dipolar cycloaddition of azomethine reaction to introduce bromo functional groups. The peripheral bromo functional groups can be used to further react with AB-type monomers through Suzuki polycondensation to afford the PF-functionalized MWCNTs, which are of a cable-like structure. Through covalent connection to MWCNTs, the fluorescence of polyfluorenes was completely quenched by the MWCNTs, indicating a fast photo-induced electron transfer from polyfluorenes to MWCNTs. 相似文献
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Conformational Investigations by Means of 13C-N.M.R.Spectroscopy. IV. Additive Calculation of the 13C-N.M.R. Chemical Shifts in 2-Bromo-cycloalkanoles and 2-Bromo-1-methoxy-cycloalkanes of Different Ring Size The 13C-n.m.r. spectra of a series of bromo-cycloalkanes, cycloalkanoles, methoxy-cycloalkanes, trans-2-bromo-cycloalkanoles and trans-2-bromo-1-methoxy-cycloalkanes (ring size n = 5, 6, 7, 8, 12) as well as cis-2-bromo-cyclododecanol and cis-2-bromo-1-methoxycyclododecane are obtained and assigned. The 13C-chemical shifts of the monosubstituted compounds have been used to estimate the substituent effects of bromo, hydroxy and methoxy groups to the α-, β- and γ-position. Using these shift parameters, the 13C-chemical shifts of the vicinal disubstituted compounds are calculated in an additive incremental manner. These 13C-chemical shifts have been compared with the experimental values and the differences are discussed with respect to the magnitude of the deviations from additivity with the dimension of steric and electronic interaction of the vicinal substituents. 相似文献
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Okamoto A Tanaka K Fukuta T Saito I 《Chembiochem : a European journal of chemical biology》2004,5(7):958-963
We report on a new method for the detection of a base at a specific site in a DNA sequence by monitoring the fluorescence emission of fluorescein. To achieve this goal, we developed a new base-discriminating fluorescent (BDF) nucleobase, naphthodeazaadenine ((ND)A). The fluorescence spectrum of the duplex possessing a cytosine base as a complementary base of (ND)A showed a fluorescence peak at 383 nm when using an excitation wavelength of 350 nm. When the complementary base of (ND)A was one of the other bases, the fluorescence intensity was very low. The fluorescence emission spectrum of (ND)A overlapped with the fluorescence excitation spectrum of fluorescein in the wavelength range of 400-500 nm. Thus, we designed FRET-BDF probes containing (ND)A as the FRET donor and fluorescein as the acceptor. The interaction of these two fluorophores, which are separated by defined base pairs, allowed an efficient energy transfer that resulted in a dominant fluorescence emission of fluorescein at 520 nm when using an excitation wavelength of 350 nm. Fluorescence emission from FRET-BDF probes was observed only when the complementary base of (ND)A is C, thus achieving a clear distinction of a C base on the complementary DNA strand. However, the general utility of our method is limited due to the quenching of the (ND)A fluorescence by a G/C base pair flanking (ND)A. 相似文献