Synthesis and First Hyperpolarizabilities of Acceptor-substituted β-apo-8'-Carotenal Derived Compounds
The synthesis and second-order nonlinear optical properties of acceptor-substituted biologically derived β-apo-8'-carotenal compounds are reported; electric field-induced second harmonic generation (EFISH) measurements give value of β(0) which are 2-6 tim
Gilmour, Sandra,Marder, Seth R.,Tiemann, Bruce G.,Cheng, Lap-Tak
Dicyano and pyridine derivatives of β-carotene: Synthesis and vibronic, electronic, and photophysical properties
Density functional theory and time-dependent density functional theory calculations provide pictures of the molecular orbitals involved in the ground and excited states of two cyano derivatives of 8′-apo-β-caroten- 8′-al synthesized via an acid-base-catal
Cruz,Siam,Rillema
experimental part
p. 1108 - 1116
(2011/05/06)
AM1 Electron Density and NMR Spectral Studies of Carotenoids with a Strong Terminal Electron Acceptor
NMR spectral analyses of 7',7'-dicyano-7'-apo-β-carotene (1), which was synthesized to assess the effect of a terminal strong electron acceptor on the structure of carotenoids and the molecular features which control their photochemical properties, are pr
Hand, Elli S.,Belmore, Kenneth A.,Kispert, Lowell D.
p. 659 - 663
(2007/10/02)
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