Poly[[µ-aqua-triaqua-[µ(6)-1,3,4,6-tetra-kis-(carboxyl-atometh-yl)-7,8-diphenyl-glycoluril]dizinc] monohydrate].

In the crystal structure of the title coordination polymer, {[Zn(2)(C(24)H(18)N(4)O(10))(H(2)O)(4)]·H(2)O}(n), the mol-ecular building block (MBB), viz [Zn(2)(CO(2))(4)(H(2)O)(4)], comprises two Zn(II) cations, each bridged by three carboxyl-ate groups from different ligand mol-ecules. These two Zn(II) cations exhibit different coordination environments: a distorted trigonal-pyramidal coordination, as an inter-mediate, is formed by the two coordinated water mol-ecules and three carboxyl-ate groups, and a distorted octa-hedral geometry defined by three water mol-ecules and three carboxyl-ate groups, in which two carboxyl-ate groups from the same side of the clip glycoluril ring and one water mol-ecule are bidentate bridging, whereas others are monodentate units. Every ligand mol-ecule connects four MBBs, thus forming a three-dimensional structure. Extensive intra- and inter-molecular O-H⋯O hydrogen bonding is observed.

Poly[[bis-(dimethyl-formamide)[µ(7)-5,5'-(methyl-enedi-oxy)diisophthalato]dizinc] dimethyl-formamide monosolvate].

In the crystal structure of the title coordination polymer, {[Zn(2)(C(17)H(8)O(10))(C(3)H(7)NO)(2)]·C(3)H(7)NO}(n), the mol-ecular build-ing block (MBB), viz. {Zn(2)(CO(2))(4)(C(3)H(7)NO)(2)}, comprises two zinc atoms, each bridged by three carboxyl-ate groups. These two Zn atoms exhibit different coordination environments: a distorted coordination intermediate between trigonal-pyramidal, and square-pyramidal formed by the two coordinated dimethyl-formamide mol-ecules and three carboxylate groups, and a distorted tetra-hedral coordination defined by carboxy-late groups of which three are bidentate bridging and the fourth is a monodentate ligand. Thus, each ligand connects four MBBs, forming the three-dimensional polymer.

catena-Poly[[bis-(pyridine-κN)zinc(II)]-µ-benzene-1,4-dicarboxyl-ato-κO:O].

In the title coordination polymer, [Zn(C(8)H(4)O(4))(C(5)H(5)N)(2)](n), the Zn(II) atom, located on a twofold rotation axis, is tetra-coordinated by two monodentate O atoms from two different carboxyl-ate groups and two pyridyl N atoms, forming a distorted tetra-hedral geometry. The Zn(II) atoms are bridged by terephthalate ligands, generating an infinite zigzag chain along [101].

Interaction of water-soluble cationic porphyrin with anionic surfactant.

The interaction of a cationic water-soluble porphyrin, 5,10,15,20-tetrakis [4-(3-pyridiniumpropoxy)phenyl]porphyrin tetrakisbromide (TPPOC3Py), with anionic surfactant, sodium dodecyl sulfate (SDS), in aqueous solution has been studied by means of UV-vis, (1)H NMR, fluorescence, circular dichroism (CD) spectra and dynamic laser light scattering (DLLS), and it reveals that TPPOC3Py forms porphyrin-surfactant complexes (aggregates), including ordered structures J- and H-aggregates, induced by association with surfactant monomers below the SDS critical micelle concentration (cmc), and forms micellized monomer upon the cmc, respectively. The position of TPPOC3Py in the micelle is determined, which is not in the micelle core instead of intercalated among the SDS chains, most likely with the pyridinium group extending into the polar headgroup region of the micelle.

Study on the inclusion behavior between meso-tetrakis[4-(3-pyridiniumpropoxy)phenyl]prophyrin tetrakisbromide and beta-cyclodextrin derivatives in aqueous solution.

The interaction of a cationic water-soluble porphyrin, 5,10,15,20-tetrakis[4-(3-pyridiniumpropoxy)phenyl]prophyrin tetrakisbromide (TPPOC3Py), with beta-CD and HP-beta-CD in aqueous solution has been studied by UV-vis, 1H NMR, 2D-NOESY and MALDI-TOF MS, and it reveals that a stable 1:1 inclusion complex between TPPOC3Py and HP-beta-CD or beta-CD has formed, in which one of the meso substituents of porphyrin ring has deeply penetrated through the cavity of HP-beta-CD from secondary face. The inclusion constants of the complexes of TPPOC3Py-beta-CD and TPPOC3Py-HP-beta-CD are (1.6+/-0.2)x10(3) M-1 and (8.9+/-0.4)x10(4) M-1, respectively.