Issue 5, 2008

A chiral C3-symmetric hexanuclear triangular-prismatic copper(ii) cluster derived from a highly modular dipeptidic N,N′-terephthaloyl-bis(S-aminocarboxylato) ligand

Abstract

The enantiomeric dipeptidic ligand N,N′-terephthaloyl-bis(L-phenylalaninato) (TBPhe2–) reacts with copper(II) acetate in ethanol under the formation of the hexanuclear double-layered triangular-prismatic cluster [Cu24-TBPhe-κO : κO′ : κO″ : κO′″)2(EtOH)(H2O)]3·∼28(H2O/0.33EtOH) with C3-symmetry, homochiral conformer assembly in the crystal and strong antiferromagnetic coupling within the Cu2(O2CR)4 paddle-wheel unit (J = −214 K).

Graphical abstract: A chiral C3-symmetric hexanuclear triangular-prismatic copper(ii) cluster derived from a highly modular dipeptidic N,N′-terephthaloyl-bis(S-aminocarboxylato) ligand

Supplementary files

Article information

Article type
Communication
Submitted
07 Nov 2007
Accepted
03 Jan 2008
First published
23 Jan 2008

CrystEngComm, 2008,10, 461-464

A chiral C3-symmetric hexanuclear triangular-prismatic copper(II) cluster derived from a highly modular dipeptidic N,N′-terephthaloyl-bis(S-aminocarboxylato) ligand

B. Wisser, A. Chamayou, R. Miller, W. Scherer and C. Janiak, CrystEngComm, 2008, 10, 461 DOI: 10.1039/B717207A

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