TY - JOUR
T1 - Supramolecular networks of octahydroxy porphyrins
AU - Bhyrappa, P.
AU - Wilson, Scott R.
AU - Suslick, Kenneth S.
N1 - We thank Teresa Prussak for technical assistance in solving the crystal structures. This work was supported by the National Institute of Health (HL 5RO1-25934).
PY - 1998
Y1 - 1998
N2 - Multifunctionalized octahydroxy porphyrins, 5,10,15,20-tetrakis(2′,6′-dihydroxyphenyl)-porphyrin, H2T(2′,6′-DHP)P, and 5,10,15,20-tetrakis-(3′,5′-dihydroxyphenyDporphyrin, H2T(3′,5′-DHP)P, have been developed as solid state building blocks for the self-assembly of hydrogen bonded supramolecular networks. A series of solid state X-ray structures of these porphyrins with various solvates show strong inter-porphyrin interactions through their peripheral hydroxyl substituents by means of directional hydrogen bonding. The position of the hydroxyl groups and the nature of the lattice guest (i.e., solvate) have dramatic influences on the molecular packing and the porosity of the structures. In particular, with ethyl acetate as solvate, the crystal structure of H2T(3′,5′-DHP)P exhibits a one dimensional columnar network, whereas H2T(2′,6′-DHP)P shows essentially a two dimensional, hydrogen-bonded, layered structure. With benzonitrile as solvate, the structure of H2T(3′,5′-DHP)P changes substantially to a two dimensional corrugated structure in order to accommodate a larger pore size. The pore volumes filled by solvate in these structures are exceptionally large: 56%, 61%, and 67% of the unit cell volume, respectively. Crystal structure data for H2T(3′,5′-DHP)P • 5 EtOAc: C64H70N4O18, M = 1183.24, triclinic, P1, a = 7.245 (2) Å, b = 14.727 (3) Å, c = 14.835 (4) Å, α = 90.18 (2)°, β= 92.90 (2)° and γ = 90.02 (2)°, V = 1580.8(7) A3, Z = 1; R1 =0.113, wR2 = 0.280 (on 2588, I > 2σr(I) observed data). For H2T(2′,6′-DHP)P • 4 EtOAc: C60H62N4O16, M = 1095.14, triclinic, P1, a = 13.736 (3) Å, b = 14.032 (3) Å, c = 17.029 (3) Å, α = 93.77 (3)°, β=110.92 (3)° and γ = 111.81 (3)°, V = 2770.9 (10) A3, Z = 2; R1 = 0.045, wR2 = 0.112 (on 6260, I > 2σ(I) observed data). For H2T(3′,5′-DHP)P • 7 C7H5N: C93H65N11O8, M = 1464.56, monoclinic, P21/m, a = 11.105 (4) Å, b= 25.744 (7) Å, c = 14.022 (3) Å, β=108.09 (2)°, V = 3811(2) A3, Z = 2; R1 = 0.062, wR2 = 0.130 (on 2588, I > 2σ(I) observed data).
AB - Multifunctionalized octahydroxy porphyrins, 5,10,15,20-tetrakis(2′,6′-dihydroxyphenyl)-porphyrin, H2T(2′,6′-DHP)P, and 5,10,15,20-tetrakis-(3′,5′-dihydroxyphenyDporphyrin, H2T(3′,5′-DHP)P, have been developed as solid state building blocks for the self-assembly of hydrogen bonded supramolecular networks. A series of solid state X-ray structures of these porphyrins with various solvates show strong inter-porphyrin interactions through their peripheral hydroxyl substituents by means of directional hydrogen bonding. The position of the hydroxyl groups and the nature of the lattice guest (i.e., solvate) have dramatic influences on the molecular packing and the porosity of the structures. In particular, with ethyl acetate as solvate, the crystal structure of H2T(3′,5′-DHP)P exhibits a one dimensional columnar network, whereas H2T(2′,6′-DHP)P shows essentially a two dimensional, hydrogen-bonded, layered structure. With benzonitrile as solvate, the structure of H2T(3′,5′-DHP)P changes substantially to a two dimensional corrugated structure in order to accommodate a larger pore size. The pore volumes filled by solvate in these structures are exceptionally large: 56%, 61%, and 67% of the unit cell volume, respectively. Crystal structure data for H2T(3′,5′-DHP)P • 5 EtOAc: C64H70N4O18, M = 1183.24, triclinic, P1, a = 7.245 (2) Å, b = 14.727 (3) Å, c = 14.835 (4) Å, α = 90.18 (2)°, β= 92.90 (2)° and γ = 90.02 (2)°, V = 1580.8(7) A3, Z = 1; R1 =0.113, wR2 = 0.280 (on 2588, I > 2σr(I) observed data). For H2T(2′,6′-DHP)P • 4 EtOAc: C60H62N4O16, M = 1095.14, triclinic, P1, a = 13.736 (3) Å, b = 14.032 (3) Å, c = 17.029 (3) Å, α = 93.77 (3)°, β=110.92 (3)° and γ = 111.81 (3)°, V = 2770.9 (10) A3, Z = 2; R1 = 0.045, wR2 = 0.112 (on 6260, I > 2σ(I) observed data). For H2T(3′,5′-DHP)P • 7 C7H5N: C93H65N11O8, M = 1464.56, monoclinic, P21/m, a = 11.105 (4) Å, b= 25.744 (7) Å, c = 14.022 (3) Å, β=108.09 (2)°, V = 3811(2) A3, Z = 2; R1 = 0.062, wR2 = 0.130 (on 2588, I > 2σ(I) observed data).
KW - Clathrate
KW - Hydrogen bonding
KW - Network solids
KW - Porphyrins
UR - https://www.scopus.com/pages/publications/0032343678
UR - https://www.scopus.com/pages/publications/0032343678#tab=citedBy
U2 - 10.1080/10610279808034983
DO - 10.1080/10610279808034983
M3 - Article
AN - SCOPUS:0032343678
SN - 1061-0278
VL - 9
SP - 169
EP - 174
JO - Supramolecular Chemistry
JF - Supramolecular Chemistry
IS - 3
ER -