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- Hao, Fuying, et al.
(författare)
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Design, crystal structures and enhanced frequency-upconverted lasing efficiencies of a new series of dyes from hybrid of inorganic polymers and organic chromophores
- 2009
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Ingår i: Journal of Materials Chemistry. - : RSC Publishing. - 0959-9428 .- 1364-5501. ; 19:48, s. 9163-9169
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Tidskriftsartikel (refereegranskat)abstract
- A new series of hybrid dyes, trans-4-(4′-N,N-dialkylaminostyryl)-N-methyl pyridinium [Cd(SCN)3−]n [alkyl = Me(1), Et(2), Pr(3) and n–Bu(4)] have been successfully synthesized from hybrids of inorganic polymers and organic chromophores. The structures of four new hybrid dyes were characterized by single-crystal X-ray diffraction first. The particular features of the hybrid dyes are (1) the inorganic anions form isolated polymeric one-dimensional zig-zag chains of [Cd(SCN)3−]n with an extended π-conjugation system within the polymeric –[M–S–C≡N]–M… chain and high polarizabilities; and (2) the organic cationic chromophores determine their optical properties. Experimental results revealed that the TPA cross-section values and overall energy conversion efficiencies of hybrid dyes with different alkyl pendant groups have obviously increased from 1 to 4, and in particular, have been substantially enhanced compared to their corresponding iodide analogues 1′–4′. Therefore, we speculate that such increases are attributable to arrangements of infinite anionic [Cd(SCN)3−]n chains and synergic effects with chromophore cations.
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| 2. |
- Tian, Yu-peng, et al.
(författare)
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Synthesis, crystal structure and NLO properties of a novel ruthenium(II) complex with unusual coordination mode
- 2005
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Ingår i: Transition metal chemistry (Weinheim). - : Kluwer Academic Publishers. - 0340-4285 .- 1572-901X. ; 30:7, s. 778-785
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Tidskriftsartikel (refereegranskat)abstract
- A new Schiff base 4-[N-hydroxyethyl-N-(methyl)amino]benzaldehyde S-methyl dithiocarbazate (HL, where H is a dissociable proton) and the ruthenium complex [Ru(bpy)2L]PF6 (bpy = 2,2′-bipyridine) have been synthesized. The structural determinations of the ligand and its ruthenium complex, by X-ray crystallography, show that the ligand is coordinated as a monoanionic bidentate N, S-donor, forming a four-member chelate ring with a bite angle of 65.91°. The complex shows intense MLCT transitions in the visible region. Fluorescent and electrochemical properties have been also studied. The complex in DMF solution exhibited a strong two-photon absorption (t.p.a.) at 532 nm nanosecond laser pulses. The t.p.a. coefficient β, t.p.a. cross-section σ and the third-order optical nonlinearity χ(3) of the complex and the ligand have been determined by the Z-scan technique.
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| 3. |
- Zhang, Xuanjun, et al.
(författare)
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Self-assembly of Organic Chromophore with Cd-S Nanoclusters: Supramolecular Structures and Enhanced Emissions
- 2005
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Ingår i: Crystal Growth & Design. - : American Chemical Society (ACS). - 1528-7483 .- 1528-7505. ; 5:2, s. 565-570
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Tidskriftsartikel (refereegranskat)abstract
- By combination of the large organic cation [trans-4-(4-dimethylanilino-styryl)-N-methyl-pyridinium with nanocluster anions ([Cd4(SC6H5)10]2- for compound 1 and [Cd4(SC6H5)6I4]2- for compound 2), two new hybrids were obtained and the structure of the [Cd4(SC6H5)6I4]2- cluster was first characterized by single-crystal X-ray diffraction. A novel supramolecular dimer {[Cd4(SC6H5)10]2-}2, connected via strong π−π interactions, was observed in 1, whereas every two [Cd4(SC6H5)6I4]2- clusters in 2 were linked by multiple C−H···I hydrogen bonds forming dimers, which, as building blocks, were further connected to each other via C−H···I hydrogen bonds and weak I···I interactions to form novel 1D helical chains. The UV−visible−near-IR spectra, one-photon excited photoluminescence, and two-photon pumped lasing were measured. The organic chromophore exhibits enhanced PL and two-photon pumped lasing in the two hybrids
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