1616558-96-3

Basic information

• Product Name: C₂₇H₃₂N₂OS
• Synonyms: C₂₇H₃₂N₂OS
• CAS NO: 1616558-96-3
• Molecular Weight: 432.63
• Mol File: 1616558-96-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: C₂₇H₃₂N₂OS(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₇H₃₂N₂OS(1616558-96-3)
• EPA Substance Registry System: C₂₇H₃₂N₂OS(1616558-96-3)

Safety Data

• Hazardous Substances Data: 1616558-96-3(Hazardous Substances Data)

Upstream product

• 98-03-3 thiophene-2-carbaldehyde 
• 90-93-7 4,4'-bis(diethylamino)benzophenone 
• 1616558-95-2 C₂₆H₃₂N₂S 
• 68-12-2 N,N-dimethyl-formamide 
• 149248-39-5 diethyl bis-(4-(diethylamino) phenyl)methylphosphonate 
• 134-91-8 4,4'-bis(N,N-diethylamino)benzhydrol 

Relevant articles and documents

With double-to the body structure of the organic second-order non-linear optical chromophore and synthetic method and use (by machine translation)

The present invention has offered a kind of double-to the body structure of the organic second-order non-linear optical chromophore, the with double to the body structure of the organic second-order non-linear optical chromophore has the following structure: Wherein R1 Is methyl or trifluoromethyl; R2 Is alkyl or phenyl. The invention used with a two-to the body structure of the electron donor, conjugated π electronic bridge and electronic receptor are combined together in the molecule after the electronic transmission capacity, can improve the electro-optic coefficient. In addition, the synthesized chromophores with double to the body structure, can effectively reduce the intermolecular interaction force. The said organic second order non-linear optical chromophore with amorphous polycarbonate doped for synthetic polymer film, the polymer film can be used as a synthetic light signal modulation material. (by machine translation)

The synthesis of new double-donor chromophores with excellent electro-optic activity by introducing modified bridges

A series of chromophores y1-y3 based on the same bis(N,N-diethyl)aniline donor and the tricyanofuran acceptor (TCF) linked together via the modified thiophene π-conjugation with different isolated groups have been synthesized and systematically investigated in this paper. Density functional theory (DFT) was used to calculate the HOMO-LUMO energy gaps and first-order hyperpolarizability (β) of these chromophores. Besides, to determine the redox properties of these chromophores, cyclic voltammetry (CV) experiments were performed. After introducing the isolation group into the thiophene, reduced energy gaps of 1.03 and 1.02 eV were obtained for chromophores y2 and y3, respectively, much lower compared to chromophore y1 ( Δ E = 1.13 eV). These chromophores showed better thermal stability with their decomposition temperatures all above 220 °C. Besides, compared with results obtained from the chromophore (y1) without the isolated group, these new chromophores show better intramolecular charge-transfer (ICT) absorption. Most importantly, the high molecular hyperpolarizability (b) of these chromophores can be effectively translated into large electro-optic (EO) coefficients (r33) in poled polymers. The electro-optic coefficient of poled films containing 25% wt of these new chromophores doped in amorphous polycarbonate (APC) afforded values of 149, 139 and 125 pm V-1 at 1310 nm for chromophores y1-y3, respectively. Besides, when the concentration was increased, the film containing chromophores y1 and y3 showed obvious phase separation, while the film with chromophore y2 showed the maximum r33 value of 146 pm V-1. Moreover, the electro-optic film prepared with these new chromophores showed greater stability. High r33 values indicated that the double donors of the bis(N,N-diethyl)aniline unit can efficiently improve the electron-donating ability and the isolated groups on the thiophene bridge can reduce intermolecular electrostatic interactions, thus enhancing the macroscopic EO activity. These properties, together with the good solubility, suggest the potential use of these new chromophores as advanced material devices.

Synthesis and optical nonlinear property of Y-type chromophores based on double-donor structures with excellent electro-optic activity

New Y-type chromophores FTC-yh1 and FTC-yh2 containing bis(N,N-diethyl) aniline as a novel electron-donor, thiophene as a π-conjugated bridge and tricyanofuran (TCF) as an acceptor have been synthesized and systematically investigated in this paper. Density functional theory (DFT) was used to calculate the HOMO-LUMO energy gaps and first-order hyperpolarizability (β) of these chromophores. These chromophores showed better thermal stability with their decomposition temperatures all above 240 °C. Most importantly, the high molecular hyperpolarizability of these chromophores can be effectively translated into large electro-optic (EO) coefficients (r33) in poled polymers. The doped film-A containing 25 wt% chromophore FTC-yh1 displayed a value of 149 pm V-1 at 1310 nm, and the doped film-B containing FTC-yh2 showed a value of 143 pm V-1 at the concentration of 25 wt%. These values are almost four times higher than the EO activity of usually reported traditional single (N,N-diethyl)aniline nonlinear optical (NLO) chromophores FTC. High r33 values indicated that the double donors of the bis(N,N-diethyl)aniline unit can efficiently improve the electron-donating ability and reduce intermolecular electrostatic interactions, thus enhancing the macroscopic EO activity. These properties, together with the good solubility, suggest the potential use of the new chromophores as advanced material devices.