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Chemistry of 1,3-Dioxepins. XIV.1 Structural Studies of 4,7-Dihydro-(4,7-dihydro-1,3-dioxepin-2-yl)-1,3-dioxepin and Their Metal Complexes (CROSBI ID 83841)

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Matak-Vinković, Dijana ; Vinković, Mladen ; Dumić, Miljenko Chemistry of 1,3-Dioxepins. XIV.1 Structural Studies of 4,7-Dihydro-(4,7-dihydro-1,3-dioxepin-2-yl)-1,3-dioxepin and Their Metal Complexes // Croatica chemica acta, 72 (1999), 2-3; 28931-x

Podaci o odgovornosti

Matak-Vinković, Dijana ; Vinković, Mladen ; Dumić, Miljenko

engleski

Chemistry of 1,3-Dioxepins. XIV.1 Structural Studies of 4,7-Dihydro-(4,7-dihydro-1,3-dioxepin-2-yl)-1,3-dioxepin and Their Metal Complexes

The coordination properties and conformational behaviour of 4,7-dihydro-(4,7-dihydro-1,3-dioxepin-2-yl)-1,3-dioxepin [1, bis-(1,3-dioxepin), or C10H14O4] were investigated. The crystal and molecular structures of bis-(1,3-dioxepin) (1), bis-(1,3-dioxepin) lithium-perchlorate (2:1) (2) and bis-(1,3-dioxepin) sodium-perchlorate (1:1) (3) complexes, as well as bis-(1,3-dioxepin) hexsaaquomagnesium-perchlorate (3:1) chlatrate (4), have been determined by X-ray diffraction. . The molecule of bis-(1,3-dioxepin) is bidentate ligand in mononuclear lithium complex 2, in contrast to its bridging mode in 2D polymeric sodium complex 3. The coordination environment around lithium in 2 is distorted octahedral with C2 symmetry, while around sodium in 3 is quasi-pentagonal bipyramidal. Out of four possible conformations of bis-(1,3-dioxepin) molecule, twist-boat-twist-boat centrosymmetric (tb-tb-c), twist-boat-twist-boat non-centrosymmetric (tb-tb), twist-boat-chair (tb-ch) and chair-chair (ch-ch), three of them are found in investigated crystal structures: ch-ch in 1, tb-tb in 2 and tb-tb-c in 3 and 4.

X-ray; 1;3-dioxepin; conformation

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Podaci o izdanju

72 (2-3)

1999.

28931-x

objavljeno

0011-1643

Povezanost rada

Kemija

Indeksiranost