排序方式: 共有80条查询结果,搜索用时 15 毫秒
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Sheng Fu Wang Yi Yuan Yu‐Chen Wei Wei‐Hsiang Chan Li‐Wen Fu Bo‐Kang Su I‐Yun Chen Keh‐Jiunh Chou Po‐Ting Chen Hsiu‐Fu Hsu Chang‐Lun Ko Wen‐Yi Hung Chun‐Sing Lee Pi‐Tai Chou Yun Chi 《Advanced functional materials》2020,30(30)
Near‐infrared organic light‐emitting diodes (NIR OLEDs) enable many unique applications ranging from night‐vision displays and photodynamic therapies. However, the development of efficient NIR OLEDs with a low efficiency roll‐off is still challenging. Here, a series of new heteroleptic Pt(II) complexes ( 1 – 4 ) flanked by both pyridyl pyrimidinate and functional azolate chelates are synthesized. The reduced ππ* energy gap of the pyridyl pyrimidinate chelate, and strong intermolecular interaction and high crystallinity in vacuum‐deposited thin films engender strong intermolecular charge transfer transition including metal–metal‐to‐ligand charge transfer; thereby, exhibiting efficient photoluminescence within 776–832 nm and short radiative lifetimes of 0.52–0.79 µs. Consequently, nondoped NIR‐emitting OLEDs based on these Pt(II) complexes are fabricated, to which Pt(II) complexes 2 and 4 give record high maximum external quantum efficiency of 10.61% at 794 nm and 9.58% at 803 nm, respectively. Moreover, low efficiency roll‐off is also observed, among which the device efficiencies of 2 and 4 are at least four times higher than that of the best NIR‐emitting OLEDs recorded at current density of 100 mA cm?2. 相似文献
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五种杀虫剂对小菜蛾的室内生物活性研究 总被引:10,自引:0,他引:10
小菜蛾Plutella xylostella是十字花科蔬菜的主要害虫,其造成的为害给蔬菜生产带来巨大损失。本文采用触杀毒力法和摄食毒力法测定了5种新颖的杀虫剂对小菜蛾的室内生物活性,研究结果表明:采用浸渍法处理72h,10%溴虫腈乳油和5.44%丁烯氟虫腈乳油对小菜蛾的触杀活性较好,其LC50值分别为1.758mg/L和2.289mg/L;采用药膜法处理72h,5.44%丁烯氟虫腈乳油和5%锐劲特悬浮剂对小菜蛾表现出了优越的胃毒作用活性,其LC50值分别为0.165mg/L和0.259mg/L。 相似文献
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以氟螨嗪为先导化合物,设计、合成了4个四嗪吡唑类新化合物,通过1~H NMR、元素分析确证了结构。对螨卵的活性测定结果显示,在10 mg/L质量浓度下,新化合物9a、9b对朱砂叶螨螨卵活性分别为86%、83%,远高于对照药剂氟螨嗪。 相似文献
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Bis‐Tridentate Ir(III) Metal Phosphors for Efficient Deep‐Blue Organic Light‐Emitting Diodes
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Hsin‐Hung Kuo Yi‐Ting Chen Leon R. Devereux Chung‐Chih Wu Mark A. Fox Chu‐Yun Kuei Yun Chi Gene‐Hsiang Lee 《Advanced materials (Deerfield Beach, Fla.)》2017,29(33)
Emissive Ir(III) metal complexes possessing two tridentate chelates (bis‐tridentate) are known to be more robust compared to those with three bidentate chelates (tris‐bidentate). Here, the deep‐blue‐emitting, bis‐tridentate Ir(III) metal phosphors bearing both the dicarbene pincer ancillary such as 2,6‐diimidazolylidene benzene and the 6‐pyrazolyl‐2‐phenoxylpyridine chromophoric chelate are synthesized. A deep‐blue organic light‐emitting diode from one phosphor exhibits Commission Internationale de l'Eclairage (CIE(x ,y )) coordinates of (0.15, 0.17) with maximum external quantum efficiency (max. EQE) of 20.7% and EQE = 14.6% at the practical brightness of 100 cd m?2. 相似文献
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Vitor RF Correia I Videira M Marques F Paulo A Costa Pessoa J Viola G Martins GG Santos I 《Chembiochem : a European journal of chemical biology》2008,9(1):131-142
Two novel families of pyrazolyl-diamine ligands that bear an anthracen-9-yl group as a DNA-binding fragment, pz*(CH2)2NH(CH2)2NHCH2-9-anthryl (pz*=pz (L(1)), 3,5-Me2pz (L2)) and pz*(CH2)2NH(CH2)2NH(2 (pz*=4-(9-anthrylmethyl)pz (L3), 3,5-Me2-4-(9-anthrylmethyl)pz (L4)), have been prepared and fully characterised. In the case of L2-L4, the evaluation of their coordination capability towards the fac-[Re(CO)3]+ core led to the synthesis of the organometallic complexes fac-[Re(CO)(3){3,5-Me(2)pz(CH2)2NH(CH2)2NHCH2-9-anthryl}]Br (7) and fac-[Re(CO)3{4-(9-anthrylmethyl)pz*(CH2)2NH(CH2)2NH2}]Br (pz*=pz (8), 3,5-Me2pz 9). The interaction of the novel pyrazole-diamine ligands and the rhenium(I) complexes with calf thymus (CT) DNA has been investigated with a variety of spectroscopic techniques (UV-visible, fluorescence, circular dichroism (CD) and linear dichroism (LD)). All of the evaluated compounds have a moderate affinity to CT DNA (3.46x10(3)相似文献
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4‐Halogeno‐3,5‐dimethyl‐1H‐pyrazole‐1‐carbodithioates: versatile reversible addition fragmentation chain transfer agents with broad applicability
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James Gardiner Ivan Martinez‐Botella Thomas M Kohl Julia Krstina Graeme Moad Jason H Tyrell Michelle L Coote John Tsanaktsidis 《Polymer International》2017,66(11):1438-1447
Pyrazole‐based dithiocarbamates are versatile reversible addition fragmentation chain transfer (RAFT) agents that provide molar mass and dispersity (? ) control over the radical polymerization of both more and less activated monomers (MAMs and LAMs). In this paper we report on theoretical and experimental findings demonstrating that their activity as RAFT agents can be significantly enhanced by introducing electron‐withdrawing substituents to the pyrazole ring. This enhancement is most noticeable in methyl methacrylate polymerization where product molar masses are more accurately predicted by the RAFT agent concentration, and significantly lower ? values, with respect to those seen with the parent RAFT agent under similar conditions, are observed. Thus, use of 4‐chloro‐3,5‐dimethyl‐1H ‐pyrazole‐1‐carbodithioate provides a poly(methyl methacrylate) with the anticipated molar mass and ? as low as 1.3 at high monomer conversion. Good control is retained for monosubstituted MAMs, styrene, methyl acrylate and N ,N ‐dimethylacrylamide. Low dispersities and less molar mass control are also achieved for homo‐ and copolymerizations with the LAM vinyl acetate, albeit with some retardation. © 2017 The Authors. Polymer International published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry. 相似文献