z-logo
Premium
Molecular Structures of Dipeptide–Palladium(II) Conjugated Complexes
Author(s) -
Moriuchi Toshiyuki,
Morimoto Kunihiro,
Sakamoto Yuki,
Hirao Toshikazu
Publication year - 2012
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201200155
Subject(s) - dipeptide , chemistry , palladium , conjugated system , ligand (biochemistry) , molecule , hydrogen bond , acetonitrile , stereochemistry , intermolecular force , crystal structure , crystallography , peptide , organic chemistry , catalysis , receptor , biochemistry , polymer
The chiral tridentate 2,6‐pyridinedicarboxamide ligand L 1 H 2 bearing two dipeptide chains (‐ L ‐Ala‐ L ‐Pro‐NHBu) was designed. Complexation of L 1 H 2 with Pd(OAc) 2 was demonstrated to afford the dipeptide–palladium(II) conjugated complex [(L 1 )Pd(MeCN)] ( 1 ) with an ancillary acetonitrile ligand. In the crystal packing of 1 , a right‐handed helical‐like molecular arrangement was observed, wherein each assembly is connected through continuous intermolecular hydrogen bonds together with water molecules. The dipeptide–palladium(II) conjugated complex 1 was studied as a metalloreceptor through metal coordination to accommodate a guest ligand, 4‐aminopyridine, resulting in the formation of the dipeptide–palladium(II) conjugated complex [(L 1 )Pd(4APy)] ( 2 ). Each preorganized helical molecule of 2 is packed in a right‐handed helical‐like molecular arrangement in the crystal packing. The dipeptide–palladium(II) conjugated complex 2 was found to exhibit emission with a maximum at 652 nm in the solid state.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom