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Royal Society of Chemistry, CrystEngComm, 30(15), p. 5961

DOI: 10.1039/c3ce00044c

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Directed self-assembly of mono and dinuclear copper(II) isophthalates into 1D polymeric structures. Design and an unusual cocrystallization

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This paper is available in a repository.

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Abstract

New examples of 1D coordination polymers containing mononuclear and dinuclear copper(II) complexes with a series of isophthalates have been designed, synthesized and characterized by single-crystal X-ray diffraction. The reaction between the aqua-complex [Cu(tmen)(H2O)x][ClO4]2 (tmen = N,N,N′,N′-tetramethylethylenediamine) and isophthalate 5-Xip (substituted in position 5, X = –H, –NO2) results in infinite chains with stoichiometry [Cu(tmen)(5-Xip)(H2O)]n. A charge-assisted hydrogen bond of type Cu–OH2O organizes the 1D chains into 2D layers. On the other hand, the self-assembly of the complex [Cu(tmen)(H2O)x][ClO4]2 with a series of isophthalates 5-Xip dianion (X = –H, –NO2, –NH2, –OMe) in presence of 0.5 equiv. of KOH results in 1D chains with dinuclear complexes [Cu2(tmen)2(μ-OH)]+3 as building blocks. The absence of a water molecule coordinated to Cu(II) atom in the dinuclear chains generates different patterns into 2D. The reaction of the aqua-complex of Cu(II) with tetrafluoroisophthalate (TFip) gave a new Janus complex [Cu2(tmen)2(H2O)2(TFip)2]·[Cu(tmen)(TF-ip)]n·3(H2O), where two different supramolecular arrangements are present in the same single crystal (a dimeric structure and 1D polymeric structure).