Title of article
Indications towards a stereoselectivity of the salt-induced peptide formation reaction
Author/Authors
Kristof Plankensteiner، نويسنده , , Alessandro Righi، نويسنده , , Bernd M. Rode، نويسنده , , Raimundo Gargallo، نويسنده , , Joaquim Jaumot، نويسنده , , Romà Tauler، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
8
From page
649
To page
656
Abstract
Different reaction yields for l- and d-alanine in the salt-induced peptide formation (SIPF) reaction, differences in the circular dichroism spectra and the complex formation constants of the involved chlorocuprate complexes point at a stereoselective differentiation between the two stereoisomers in the SIPF reaction and give a possible explanation towards the origin of homochirality in the process of the origin of life. An explanation of the observed effects can for the time being only be based on assumptions but could possibly be related to the inherent chirality of the CuII ion as a central atom of the [CuCl(gly)(glyH2)(H2O)2]+ complex due to parity violation in weak interactions and to amplification of chirality related to the structural properties of the complex.
Keywords
Prebiotic peptide formation , Copper complexes , Amino acid complexes , Origin of homochirality , SIPF reaction , Stereoselective differentiation
Journal title
INORGANICA CHIMICA ACTA
Serial Year
2004
Journal title
INORGANICA CHIMICA ACTA
Record number
1321965
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