TY - JOUR
T1 - Coordination networks from Cu cations and tetrakis(methylthio) benzenedicarboxylic acid
T2 - Tunable bonding patterns and selective sensing for NH3 gas
AU - Zhou, Xiao-Ping
AU - Xu, Zhengtao
AU - He, Jun
AU - Zeller, Matthias
AU - Hunter, Allen D.
AU - Clérac, Rodolphe
AU - Mathonière, Corine
AU - Chui, Stephen Sin-Yin
AU - Che, Chi-Ming
PY - 2010/11/1
Y1 - 2010/11/1
N2 - This paper aims to illustrate the rich potential of the thioether-carboxyl combination in generating coordination networks with tunable and interesting structural features. By simply varying the ratio between Cu(NO3) 2 and the bifunctional ligand tetrakis(methylthio)benzenedicarboxylic acid (TMBD) as the reactants, three coordination networks can be hydrothermally synthesized in substantial yields, which present a distinct evolution with regard to metal-ligand interactions. Specifically, Cu(TMBD)0.5(H 2TMBD)0.5•H2TMBD (1) was obtained with a relatively small (1:1) Cu(NO3)2/TMBD ratio, and crystallizes as an one-dimensional (1D) coordination assembly based on Cu(I)-thioether interactions, which is integrated by hydrogen-bonding to additional H2TMBD molecules to form a three-dimensional (3D) composite network with all the carboxylic acid and carboxylate groups remaining uncoordinated to the metal ions. A medium (1.25:1) Cu(NO3) 2/TMBD ratio leads to compound Cu2TMBD, in which Cu(I) ions simultaneously bond to the carboxylate and thioether groups, while an even higher (2.4:1) Cu(NO3)2/TMBD ratio produced a mixed-cation compound CuII
2OHCuI(TMBD)2• 2H2O (2), in which the carboxylic groups are bonded to (cupric) CuII ions, and the thioether groups to CuI. Despite the lack of open channels in 2, crystallites of this compound exhibit a distinct and selective absorption of NH3, with a concomitant color change from green to blue, indicating substantial network flexibility and dynamics with regards to gas transport. © 2010 American Chemical Society.
AB - This paper aims to illustrate the rich potential of the thioether-carboxyl combination in generating coordination networks with tunable and interesting structural features. By simply varying the ratio between Cu(NO3) 2 and the bifunctional ligand tetrakis(methylthio)benzenedicarboxylic acid (TMBD) as the reactants, three coordination networks can be hydrothermally synthesized in substantial yields, which present a distinct evolution with regard to metal-ligand interactions. Specifically, Cu(TMBD)0.5(H 2TMBD)0.5•H2TMBD (1) was obtained with a relatively small (1:1) Cu(NO3)2/TMBD ratio, and crystallizes as an one-dimensional (1D) coordination assembly based on Cu(I)-thioether interactions, which is integrated by hydrogen-bonding to additional H2TMBD molecules to form a three-dimensional (3D) composite network with all the carboxylic acid and carboxylate groups remaining uncoordinated to the metal ions. A medium (1.25:1) Cu(NO3) 2/TMBD ratio leads to compound Cu2TMBD, in which Cu(I) ions simultaneously bond to the carboxylate and thioether groups, while an even higher (2.4:1) Cu(NO3)2/TMBD ratio produced a mixed-cation compound CuII
2OHCuI(TMBD)2• 2H2O (2), in which the carboxylic groups are bonded to (cupric) CuII ions, and the thioether groups to CuI. Despite the lack of open channels in 2, crystallites of this compound exhibit a distinct and selective absorption of NH3, with a concomitant color change from green to blue, indicating substantial network flexibility and dynamics with regards to gas transport. © 2010 American Chemical Society.
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U2 - 10.1021/ic101501p
DO - 10.1021/ic101501p
M3 - RGC 21 - Publication in refereed journal
C2 - 20886889
SN - 0020-1669
VL - 49
SP - 10191
EP - 10198
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 21
ER -