Issue 21, 2011

Syntheses, crystal structures and optical properties of six homochiral coordination networks based on phenyl acid-amino acids

Abstract

Six homochiral metal–organic coordination networks based on two new phenyl acid-amino acids, [ZnL112(H2O)2] (1), [Cu2L112(H2O)3] (2), [Zn2L112] (3), [CuL22(H2O)2]·2H2O (4), [ZnL22] (5) and [Cd3NaL223(ClO4)]·3H2O·DMF (6), where L11 = (S)-4-((1-carboxy-2-methylpropylamino)methyl)benzoic acid, and L22 = (S)-4-((1-carboxy-2-hydroxyethylamino)methyl)benzoic acid, have been synthesized and characterized. Compound 1 is a supramolecular network of hydrogen bondings linking up discrete zinc coordination units, and compound 2 presents a 2D lattice motif of water molecules linking up polymeric chains, while compound 3 is a 3D network constructed of interesting left-hand triple helices. Compound 4 consists of 1D coordination polymeric chains, while compound 5 adopts an intriguing 2D diamondoid network built from two kinds of left-handed helices, and compound 6 is a 3D framework constructed from homochiral cages. In addition, the second-order nonlinear optics (NLO) properties of compounds 1–6 were investigated. Compound 1 has a powder SHG intensity of 3.4 versus a-quartz, and the powder SHG intensities of compounds 2–4 approximate to that of a-quartz, while the powder SHG intensities are 7.8 and 8.4 versus a-quartz for compounds 5 and 6, respectively. Compounds 1, 3, 5 and 6 in the solid state exhibit blue fluorescent emissions at room temperature, mainly attributed to the ligand-centered transitions.

Graphical abstract: Syntheses, crystal structures and optical properties of six homochiral coordination networks based on phenyl acid-amino acids

Supplementary files

Article information

Article type
Paper
Submitted
08 Apr 2011
Accepted
20 Jul 2011
First published
24 Aug 2011

CrystEngComm, 2011,13, 6422-6430

Syntheses, crystal structures and optical properties of six homochiral coordination networks based on phenyl acid-amino acids

X. Yang, M. Xie, C. Zou and C. Wu, CrystEngComm, 2011, 13, 6422 DOI: 10.1039/C1CE05422H

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