850494-55-2Relevant academic research and scientific papers
Wavelength-dependent stereodifferentiation in the fluorescence quenching of asymmetric naphthalene-based dyads by amines
Abad, Sergio,Pischel, Uwe,Miranda, Miguel A.
, p. 2711 - 2717 (2005)
In the present contribution, wavelength has been used as a tunable parameter to achieve selective control of the photophysics of two novel asymmetric bichromophoric dyads composed of naphthalene units, i.e., 6-methoxynaphthalene (NPX) and 1-methylnaphthalene (NAP) derivatives, with different electronic properties, connected by an amide spacer [(S,S) and (S,R)-NPX-NAP]. As model systems, relevant monochromophoric compounds (NPX-M and NAP-M) have also been investigated. While upon excitation at 325 nm the light energy remained in the NPX moiety, at 290 nm an efficient singlet - singlet energy transfer (ΦSSET of about 97%) from the NAP unit to the NPX chromophore dominated. A remarkable Stereodifferentiation was observed in the excited-state quenching by triethylamine via exciplex formation. The results demonstrate that it is possible to control configuration-dependent interactions in the excited state by wavelength tuning. This can be rationalized through intramolecular interactions of π systems leading to modulation of the redox properties.
New Chiral Stationary Phases with Two Chiral Centers for the Liquid Chromatographic Resolution of Racemic Anti-inflammatory Drugs Related to α-Arylpropionic Acids
Hyun, Myung Ho,Hwang, Seung-Ryul,Ryoo, Jae-Jeong
, p. 1021 - 1024 (2007/10/02)
New chiral stationary phases (CSPs) with two chiral centers were prepared from (R)- or (S)-α-naphthylethylamine and (S)-naproxen.The (R,S)-CSP prepared from (R)-α-naphthylethylamine and (S)-naproxen was found to be very successful in resolving 3,5-dinitroanilide derivatives of antiinflammatory drugs related to α-arylpropionic acids.
