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Henri J.-M. Dou Maria Ludwikow Parina Hassanaly Jacky Kister Jacques Metzger 《Journal of heterocyclic chemistry》1980,17(2):393-395
A general study of the chemical behavior of heterocyclic anions, dianions and dianionic reagents under phase transfer catalysis conditions allowed us to synthesize various heterocyclic compounds such as imidazo[2,1-b]thiazole and derivatives; imidazo[2,1-b]thiazine and imidazo[2,1-b]benzothiazepine. Reaction conditions e.g., catalyst, solvent, temperature, etc., are indicated. 相似文献
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近年来 ,自组装及其形成的多层复合膜已经在导电、生物传感器及非线性光学等领域得到深入研究 ,特别是以聚阴离子与聚阳离子相互作用的静电自组装研究更为深入 .这一技术制备方法简单 ,无需特别的设备 ,对膜层厚度能随意调控 ,并以水作为介质 ,对环境无害 [1~ 3] .共轭高分子 (如聚苯胺、聚吡咯及聚苯亚乙烯等 )通过自组装形成共轭高分子膜 ,对制备具有导电、光电和传输等功能的薄膜半导体器件具有重要意义 .聚乙炔类是最早被发现且理论与应用研究最多的一类共轭高分子材料[4 ,5] .本文以聚 ( 4 -羧酸苯基 )乙炔 ( PCPA)为聚阴离子 ,以重… 相似文献
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Equilibrium constants for oxidations of cyclanols by cyclohexanone in benzene have been determined in the presence of aluminium isopropoxide. The free energies of the equilibrium (ΔGox) are correlated with equilibrium constants for dissociation of cyanohydrins, rate constants for cyclanol oxidation with chromic acid, ketone reduction with sodium borohydride and trifluoroethanolysis of tosylates. 相似文献
5.
Shunjie Liu Yuanyuan Li Ryan T. K. Kwok Jacky W. Y. Lam Ben Zhong Tang 《Chemical science》2021,12(10):3427
Aggregation-induced emission (AIE) is a cutting-edge fluorescence technology, giving highly-efficient solid-state photoluminescence. Particularly, AIE luminogens (AIEgens) with emission in the range of second near-infrared window (NIR-II, 1000–1700 nm) have displayed salient advantages for biomedical imaging and therapy. However, the molecular design strategy and underlying mechanism for regulating the balance between fluorescence (radiative pathway) and photothermal effect (non-radiative pathway) in these narrow bandgap materials remain obscure. In this review, we outline the latest achievements in the molecular guidelines and photophysical process control for developing highly efficient NIR-II emitters or photothermal agents with aggregation-induced emission (AIE) attributes. We provide insights to optimize fluorescence efficiency by regulating multi-hierarchical structures from single molecules (flexibilization) to molecular aggregates (rigidification). We also discuss the crucial role of intramolecular motions in molecular aggregates for balancing the functions of fluorescence imaging and photothermal therapy. The superiority of the NIR-II region is demonstrated by fluorescence/photoacoustic imaging of blood vessels and the brain as well as photothermal ablation of the tumor. Finally, a summary of the challenges and perspectives of NIR-II AIEgens for in vivo theranostics is given.Structural and process controls of NIR-II AIEgens realize manipulating of radiative (R) and nonradiative (NR) decay for precise theranostics. 相似文献
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Henri J.-M. Dou Parina Hassanaly Jacky Kister Jacques Metzger 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):355-358
Abstract Alkylation via phase transfer catalysis of several ambident anions of the |N–C–S|? type leads exclusively to S-substitution. Yields obtained are better or equal to those given by conventional methods and experimental work-up is very much simplified compared to the latter. 相似文献
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Mechanistic studies promote scientific development from phenomena to theories.Aggregation-induced emission(AIE),as an unusual photophysical phenomenon,builds the bridge between molecular science and aggregate mesoscience.With the twenty-year development of AIE,restriction of intramolecular motion(RIM)has been verified as the working mechanism of AIE effect.In this review,these mechanistic works about RIM are summarized from experimental and theoretical perspectives.Thereinto,the experimental studies are introduced from three parts:external rigidification,structural modification and structural characterization.In the theoretical part,calculations on the low-frequency motion of AIEgens have been performed to prove the RIM mechanism.By virtue of the theoretical calculations,some new mechanisms are proposed to supplement the RIM,such as restriction of access to conical intersection,suppression of Kasha transition,restriction of access to dark state,etc.It is foreseeable that the RIM mechanism will unify the photophysical theories for both molecules and aggregates,and inspire more progress in aggregate science. 相似文献
9.
Dr. Andrea Previtali Dr. Wei He Dr. Alessandra Forni Dr. Daniele Malpicci Dr. Elena Lucenti Dr. Daniele Marinotto Prof. Lucia Carlucci Prof. Pierluigi Mercandelli Dr. Marco Aldo Ortenzi Prof. Giancarlo Terraneo Dr. Chiara Botta Prof. Ryan Tsz Kin Kwok Dr. Jacky Wing Yip Lam Prof. Ben Zhong Tang Prof. Elena Cariati 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(67):16690-16700
Organic materials with multiple emissions tunable by external stimuli represent a great challenge. TTPyr, crystallizing in different polymorphs, shows a very rich photophyisics comprising excitation-dependent fluorescence and phosphorescence at ambient conditions, and mechanochromic and thermochromic behavior. Transformation among the different species has been followed by thermal and X-ray diffraction analyses and the emissive features interpreted through structural results and DFT/TDDFT calculations. Particularly intriguing is the polymorph TTPyr(HT), serendipitously obtained at high temperature but stable also at room temperature, whose non-centrosymmetric structure guarantees an SHG efficiency 10 times higher than that of standard urea. Its crystal packing, where only the TT units are strongly rigidified by π-π stacking interactions while the Pyr moieties possess partial conformational freedom, is responsible for the observed dual fluorescence. The potentialities of TTPyr for bioimaging have been successfully established. 相似文献
10.
Dr. Yuanyuan Li Dr. Shunjie Liu Huwei Ni Haoke Zhang Dr. Hequn Zhang Clarence Chuah Chao Ma Prof. Kam Sing Wong Prof. Jacky W. Y. Lam Prof. Ryan T. K. Kwok Prof. Jun Qian Prof. Xuefeng Lu Prof. Ben Zhong Tang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(31):12922-12926
The traditional design strategies for highly bright solid-state luminescent materials rely on weakening the intermolecular π–π interactions, which may limit diversity when developing new materials. Herein, we propose a strategy of tuning the molecular packing mode by regioisomerization to regulate the solid-state fluorescence. TBP-e-TPA with a molecular rotor in the end position of a planar core adopts a long-range cofacial packing mode, which in the solid state is almost non-emissive. By shifting molecular rotors to the bay position, the resultant TBP-b-TPA possesses a discrete cross packing mode, giving a quantum yield of 15.6±0.2 %. These results demonstrate the relationship between the solid-state fluorescence efficiency and the molecule's packing mode. Thanks to the good photophysical properties, TBP-b-TPA nanoparticles were used for two-photon deep brain imaging. This molecular design philosophy provides a new way of designing highly bright solid-state fluorophores. 相似文献