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首页> 外文期刊>Inorganica Chimica Acta >Organometallic complexes for nonlinear optics. Part 29. Quadratic and cubic hyperpolarizabilities of stilbenylethynyl-gold and -ruthenium complexes
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Organometallic complexes for nonlinear optics. Part 29. Quadratic and cubic hyperpolarizabilities of stilbenylethynyl-gold and -ruthenium complexes

机译:非线性光学的有机金属配合物。第29部分。苯乙烯基乙炔基金和钌络合物的二次和立方超极化率

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The compounds (E)-4-XC=CC6H4CH=CHPh [X = SiMe3 (1), H (2)],1,3,5- (E)-4-XC6H4CH CH}(3)C6H3 [X = 1 (3), C= CSiMe3 (4) C = CH (5)], [Au{(E)-4-C=CC6H4CH-CHPh}(L)] [L = PPh3 (6), PMe3 (7)], [Au(4-C=CC6H4C=CPh)(L)] [L = PPh3 (8), PMe3 (9)], 1,3,5-[(Ph3P)Au (E)-4-C=CC6H4CH=CH}](3)C6H3 (10), trans-[Ru (E)-4-C-CHC6H4CH=CHPh}Cl(dppm)(2)]PF6 (11), trans[Ru{(E)-4-C=CC6H4CH=CHPh}Cl(L-2)(2)] [L-2=dppm (12), dppe (13)], [1,3,5-(trans-[(dppm)(2)C]Ru{(E)-4-C-CHC6H4CH= CH}])(3)C6H3](PF6)(3) (14), 1,3,5-(trans-[(L-2)(2)ClRu{(E)-4-C-CC6H4CH-CH}])(3)C6H3 [L-2 = dppm (15), dppe (16)] and 1,3,5-(trans[(dppe)(2)(PhC=C)Ru (E)-4-C=CC6H4CH=CH}])(3)C6H3 (17) have been prepared (and the identity of 6 confirmed by a single-crystal X-ray diffraction study), and their electrochemical (Ru complexes) and nonlinear optical (NLO) properties assessed. The ruthenium complexes display reversible (12, 13, 15-17) or nonreversible (11, 14) processes attributable to Ru-centered oxidation, at potentials similar to those of previously-investigated monoruthenium alkynyl or vinylidene complexes. No evidence for intermetallic electronic communication in 14-17 is observed. Quadratic nonlinearities at 1064 and 800 nm for the octopolar stilbenyl-ruthenium complexes 14, 15 are large for compounds without strongly accepting substituents. Cubic molecular hyperpolarizabilities at 800 nm for the organic compounds and gold complexes are low. Cubic nonlinearities gamma(800) and two-photon absorption (TPA) cross-sections sigma(2) for the ruthenium complexes increase on proceeding from linear analogues 12, 13 to octopolar complexes 15, 16; the latter and 17 possess some of the largest gamma(800) and sigma(2) values for organometallics thus far. Cubic nonlinearities lm(chi((3))/N for 13, 16, and 17 from the first application of electroabsorption (EA) spectroscopy to organometallics are also large, scaling with the number of metal atoms. (C) 2002 Elsevier Science B.V. All rights reserved. [References: 50]
机译:化合物(E)-4-XC = CC6H4CH = CHPh [X = SiMe3(1),H(2)],1,3,5-(E)-4-XC6H4CH CH}(3)C6H3 [X = 1 (3),C = CSiMe3(4)C = CH(5)],[Au {(E)-4-C = CC6H4CH-CHPh}(L)] [L = PPh3(6),PMe3(7)] ,[Au(4-C = CC6H4C = CPh)(L)] [L = PPh3(8),PMe3(9)],1,3,5-[(Ph3P)Au(E)-4-C = CC6H4CH = CH}](3)C6H3(10),反式[Ru(E)-4-C-CHC6H4CH = CHPh} Cl(dppm)(2)] PF6(11),反[Ru {(E)-4 -C = CC6H4CH = CHPh} Cl(L-2)(2)] [L-2 = dppm(12),dppe(13)],[1,3,5-(反式-[[dppm)(2) C] Ru {(E)-4-C-CHC6H4CH = CH}])(3)C6H3](PF6)(3)(14),1,3,5-(反式[[(L-2)(2) )ClRu {(E)-4-C-CC6H4CH-CH}])(3)C6H3 [L-2 = dppm(15),dppe(16)]和1,3,5-(trans [(dppe)( 2)(PhC = C)Ru(E)-4-C = CC6H4CH = CH}])(3)C6H3(17)的制备(单晶X射线衍射研究证实为6) ,并评估了它们的电化学(Ru配合物)和非线性光学(NLO)特性。钌络合物显示出可归因于Ru中心氧化的可逆过程(12、13、15-17)或不可逆过程(11、14),其电势类似于先前研究的单钌炔基或亚乙烯基络合物。没有观察到14-17中金属间电子通信的证据。对于没有强烈接受取代基的化合物,八极苯乙烯基-钌配合物14、15在1064和800 nm处的二次非线性很大。有机化合物和金络合物在800 nm处的立方分子超极化率很低。钌配合物的立方非线性γ(800)和双光子吸收(TPA)截面sigma(2)随着线性类似物12、13到八极配合物15、16的增加而增加;后者和17具有迄今为止最大的有机金属 gamma(800)和sigma(2)值。从首次将电吸收(EA)光谱应用于有机金属以来,三次非线性lm(chi((3))/ N对于13、16和17来说也很大,与金属原子的数量成比例。(C)2002 Elsevier Science BV保留所有权利[参考:50]

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