7235-50-9Relevant academic research and scientific papers
Experimental and theoretical studies on constitutional isomers of 2, 6-dihydroxynaphthalene carbaldehydes. effects of resonance-assisted hydrogen bonding on the electronic absorption spectra
Houjou, Hirohiko,Motoyama, Takatoshi,Banno, Seisaku,Yoshikawa, Isao,Araki, Koji
scheme or table, p. 520 - 529 (2009/05/30)
We prepared and characterized a series of mono-and dicarbaldehydes of 2, 6-dihydroxynaphthalene that bear potential resonance-assisted hydrogen bonding (RAHB) unit(s). X-ray crystal structures of selected compounds revealed that each salicylaldehyde moiety forms an intramolecular hydrogen bond and that the introduction of formyl groups into either the α-or β-position causes a considerable difference in geometry, which was interpretative from a conventional scheme of resonance hybrids including ionic state. Analyses on NMR chemical shifts suggested that the compounds in solution are present as an equilibrium mixture between closed and open forms with respect to RAHB units. Ab initio calculations indicated that the formation of an intramolecular hydrogen bond strikingly influences the aromaticity of the individual local six-membered ring of naphthalene. The trend of the change in aromaticity was analyzed in connection with the extra stabilization energy of RAHB. In the UV-vis spectra, the β-formyl derivatives specifically showed a substantial red shift compared to α-formyl derivatives. The absorption features were successfully reproduced by TD-DFT calculation, and those data were consistently explained from the effects of RAHB on electronic state of the naphthalene's π-system. Finally, we pointed out a similarity in the electronic state between RAHB-bearing molecules and cata-condensed aromatic hydrocarbons. Copyright 2009 by the American Chemical Society.
INTRACAVITY ACETYL TRANSFER
Whitlock, Barbara J.,Whitlock, Howard W.
, p. 6047 - 6050 (2007/10/02)
Synthesis of water soluble cyclophane 1, designed as an esterase mimic is described.Cyclophane 1 is an effective acetyl acceptor, from water soluble acetylating agents capable of intracavity complexation.
