628700-59-4Relevant academic research and scientific papers
Cadmium(II) and zinc(II) complexes of pyrrole-appended oxacarbaporphyrin: A side-on coordination mode of O-confused carbaporphyrin
Pawlicki, Milosz,Latos-Grazynski, Lechoslaw,Szterenberg, Ludmila
, p. 9779 - 9786 (2005)
A pyrrole adduct of 5,20-diphenyl-10,15-di(p-tolyl)-2-oxa-21-carbaporphyrin [(H,pyr)OCPH]H2 reacted with sodium ethanolate to yield 5,20-diphenyl-10,15-di(p-tolyl)-3-ethoxy-3-(2′-pyrrol)-2-oxa-21- carbaporphyrin [(EtO,Pyr)OCPH]H2. Subsequently, true O-confused oxaporphyrin with a pendant pyrrole ring [(pyr)OCPH]H was formed by the addition of acid to [(EtO,pyr)OCPH]H2, which triggered an ethanol elimination. In the course of this process, the tetrahedral-trigonal rearrangements originated at the C(3) atom. Insertion of zinc(II), cadmium(II), and nickel(II) into [(pyr)-OCPH]H yielded [(pyr)OCPH]ZnIICl, [(pyr)OCPH]CdIICl, and [(pyr)OCP]NiII. The formation of [(pyr)OCP]NiII was accompanied by the C(21)H dehydrogenation step. The nickel(II) ion of [(pyr)OCP]NiII, coordinated to a dianionic macrocyclic ligand, is bound by three pyrrolic nitrogens and a trigonally hybridized C(21) atom of the inverted furan. The pyrrole-appended O-confused carbaporphyrin acts as a monoanionic ligand toward zinc(II) and cadmium-(II) cations. Three nitrogen atoms and the C(21)H fragment of the inverted furan occupy equatorial positions. In 1H NMR spectra, the unique inner C(21)H resonances of the inverted furan ring are located at 0.15 ppm for [(pyr)-OCPH]ZnIICl, and at 0.21 ppm for [(pyr)OCPH]CdIICl. The proximity of the furan fragment to the metal ion induces direct scalar couplings between the spin-active nucleus of the metal (111/113Cd) and the adjacent 1H nucleus. The interaction of the metal ion and C(21)H was also reflected by significant changes in carbon chemical shifts ([(pyr)-OCPH]ZnIICl, 78.3 ppm; [(pyr)OCPH]CdIICl, 81.4 ppm; the free base, 101.3 ppm). The density functional theory (DFT) has been applied to model the molecular structures of zinc(II) and cadmium(II) complexes of O-confused oxaporphyrin with an appended pyrrole ring. The Cd...C(21) distance in the optimized structure exceeds the typical Cd-C bond lengths, but is much shorter than the corresponding van der Waals contact.
