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[4-(2,2':5',2''-terthiophen-5-yl)phenyl]tris(trimethylsiloxy)silane is a 'donor-free' chromophore where the terthiophene unit serves as both a donor and π-spacer, while the tris(trimethylsiloxy)silane group acts as an acceptor, mimicking a silica surface fragment. [4-(2,2':5',2''-terthiophen-5-yl)phenyl]tris(trimethylsiloxy)silane exhibits strong second-order nonlinear optical (NLO) activity, outperforming nitro-substituted analogs in terms of μβEFISH values, while maintaining favorable transparency for NLO applications. The silane acceptor minimally affects the electronic properties of the terthiophene but enhances NLO performance, making it a promising candidate for optoelectronic materials.

1206964-04-6

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1206964-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206964-04-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,9,6 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1206964-04:
(9*1)+(8*2)+(7*0)+(6*6)+(5*9)+(4*6)+(3*4)+(2*0)+(1*4)=146
146 % 10 = 6
So 1206964-04-6 is a valid CAS Registry Number.

1206964-04-6Downstream Products

1206964-04-6Relevant articles and documents

Oligothiophenes nano-organized on a cyclotetrasiloxane scaffold as a model of a silica-bound monolayer: Evidence for intramolecular excimer formation

Mroz, Wojciech,Bombenger, Jean Philippe,Botta, Chiara,Biroli, Alessio Orbelli,Pizzotti, Maddalena,De Angelis, Filippo,Belpassi, Leonardo,Tubino, Riccardo,Meinardi, Francesco

, p. 12791 - 12798 (2009)

Excimer formation in a new class of terthiophene-based fluorophores covalently bonded to a cyclotetrasiloxane scaffold has been demonstrated and the photophysical process ruling it has been investigated in detail and modeled theoretically. In contrast to

A ‘donor-free’ chromophore with a silicon-based acceptor group for second order nonlinear optics

Di Carlo, G.,Fantucci, P.,Forni, A.,Orbelli Biroli, A.,Pizzotti, M.,Righetto, S.,Tessore, F.

, (2022/01/13)

In this paper we report an investigation on the linear and nonlinear properties of a non-classic push-pull molecule, based on the molecular design concept of a ‘donor-free’ chromophore. Herein a terthiophene unit acts both as a donor and a π-spacer group and a tris(trimethylsiloxy)silane substituent as an acceptor group. This latter can represent a model of a fragment of silica surface and it has been compared with a classic acceptor unit like the nitro group. The ‘donor-free’ chromophores have also been compared to more typical push-pull chromophores by replacing the terthiophene unit with the N,N-dimethylamino donor group. Despite the silane group only slightly impacts on the electronic and linear properties of the terthiophene, our results reveal high μβEFISH values for silane-functionalized derivatives producing a NLO activity stronger than that of the nitro substituted. Finally, the investigated ‘donor-free’ NLO-phore exhibits interesting physical properties relevant in term of nonlinearity/transparency trade-off, a highly desired requirement for second-order NLO materials.

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