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51.
Many advances have been made in chemical structure research over the past three decades using synchrotron radiation. Synchrotron radiation has a number of unique properties. They include high brightness, high collimation, broad energy spectrum, variable polarization, coherent power, and subnanosecond pulse width. The third-generation storage rings with wiggler and undulator sources and lower electron beam dimensions are delivering over 1012 times higher brightness than laboratory-based sources. The future of synchrotron sources looks very promising with the development of energy recovery linac sources and free-electron laser sources. These will permit dynamic studies of chemical structure with subpicosecond time resolution. Commensurate with the development of X-ray sources, major progress has occurred in optical schemes to meet the challenging needs of chemical structure research. High-resolution monochromatization and submicron focusing of X rays present new avenues for the future.  相似文献   
52.
《Arabian Journal of Chemistry》2020,13(12):8848-8887
Phthalocyanine (Pc) complexes are an important class of dyes with numerous (e.g., biological, photophysical, and analytical) applications. Among the methods used to improve the properties of these complexes, one should mention the introduction of different substituents, variation of the central metal ion, ligand exchange, and conjugation to nanomaterials (e.g., carbon-based nanomaterials and metal nanoparticles (NPs)). This work briefly reviews Pc complex conjugation to Ag and Au NPs, highlights the different NP shapes, and discusses the diversity of conjugation approaches. Moreover, the use of UV–Vis spectroscopy, powder X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, atomic force microscopy, dynamic light scattering and Fourier transform infrared spectroscopy to characterize Pc-NP hybrids is summarized. The effect of conjugation on Pc photo-physicochemical properties (fluorescence, singlet oxygen generation, triplet state formation, and optical limiting behavior) is discussed, and future perspectives for the synthesis and applications of new hybrids are provided.  相似文献   
53.
The synthesis and electronic properties of new linear organic π-conjugated systems incorporating phosphole rings are described. Well defined α,α′-(phosphole-thiophene) oligomers possess low HOMO-LUMO gaps and their optical and electrochemical properties can be tuned via chemical modifications of the P-atoms. The physical properties of these compounds make them valuable materials for OLED’s. The coordination ability of phosphole-based dipoles has been exploited for the synthesis of efficient multipolar NLO-phores. Lastly, phospholes have been used for the synthesis of assemblies exhibiting through-bond interaction between two π-systems via P-P σ-skeletons.  相似文献   
54.
The two independent elements of the second-order nonlinear optical susceptibility tensor of a range of contact poled, donor–acceptor substitued side-chain polymers are reported. The susceptibilities were measured by second harmonic generation from thin films, typically less than 0.5 μm thick, at a fundamental wavelength of 1064 nm. The largest value was χ = 2.64 pm/V which is three times greater than the χ value of KDP and was measured in a nitrobenzylidene side chain, polyhydroxystyrene polymer with an eleven unit alkyl chain spacer attaching the side group to the backbone. Typical susceptibility values obtained were χ~0.3 pm/V and X(2)33~1 pm/V. The coherence lengths of the materials, which lay in the range 4–12 μm, were measured at 1064 nm by the maker fringe technique using thick, wedge-shaped samples.  相似文献   
55.
Six isomeric C20 alkylthiophenes were synthesized in order to prove the occurrence of such compounds in various deep sea sediments. As expected from the analogy with the corresponding saturated hydrocarbons, 2- and 3-heptadecylthiophene have considerably longer relative retention times than the isomeric isoprenoid compounds, i.e. 2- and 3-(4,8,12-trimethyltridecyl)thiophene and 3- and 4-methyl-2-(3,7,11-trimethyldodecyl)thiophene. Covats retention indices for all compounds were determined by isothermal analysis at 190°C on two different silicone-coated capillary columns. The mass spectra of the monoalkylated thiophenes show a base peak at m/z 98 corresponding to a Mcafferty rearrangement product in the case of the 3-substituted isomers, whereas a simple benzylic cleavage dominates in the mass spectra of 2-alkylthiophenes. 4-Methyl-2-(3,7,11-trimethylodecy)thiophene is an exception from this simple rule because also shows the McLafferty rearrangement as dominant fragmentation. Two of the isoprenoid thiophenes are prominent compounds in various deep sea sediments.  相似文献   
56.
Further expansion of optical communication systems depends strongly on the development of cheap component technologies for functions such as switching, demultiplexing and amplification. Silica-on-silicon is increasingly recognised as the best approach to low cost integrated optics for such applications, but so far the functionality is limited. The purpose of NODES, a basic research collaboration sponsored by the European Union under the programme ESPRIT, has been to examine the application of sol-gel to a highly functional silica-on-silicon technology. In particular, the project has investigated film processing and characterisation, rare-earth doping for amplification, and semiconductor nanocrystallite doping for nonlinear functions. This paper presents the background and context to this work, summarises the technical results obtained, and discusses requirements and challenges for successful application of sol-gel in photonics.  相似文献   
57.
58.
以1,4-萘醌为原料,合成了含硫的醌构稠杂环化合物苯并[b]萘并[2',3':5,6][1,4]二噻英并[2,3-i]噻蒽-5,7,9,14,16,18-六酮(4),其结构经1H NMR和IR确证.采用波长为800 nm,脉宽为80 fs的Ti:Sapphire飞秒激光,运用双光束简并四波混频法测定了4的三阶非线性光学性能,结果表明,4的三阶非线性光学极化率χ(3),非线性折射率n2,分子二阶超极化率γ和响应时间分别为2.89×10-13 esu, 5.31×10-12 esu, 3.14×10-31 esu和101 fs.并分析了4的分子结构对其三阶非线性光学性能的影响.  相似文献   
59.
The new chromophore compounds with NLO properties were prepared by Knoevenagel condensation from forrnyl or diformyl calix[4/arene and isophorone derivatives in the presence of piperidine and acetic acid, respectively. In these chromophore calix[4]arenes, the ring locked trienes were employed as the conjugation bridge and electron acceptor in D-π-A units. The NMR spectra demonstrated that they existed in a cone conformation and consequently non-conjugated D-π-A units could be oriented at nearly the same direction.  相似文献   
60.
Synthesis of the third-order nonlinear materials:bis (1,4-dihydroxynaphthalene) tetrathiafulvalene and bis (1,4-dialkoxylnaphthalene) tetrathiafulvalene has been achieved in four steps, starting from 2,3-dichloro-1,4-naphthaquinone. The materials exhibit larger third-order nonlinear optical susceptibilities χ.  相似文献   
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