Extended lead(II) architectures engineered via tetrel bonding interactions; New Journal of Chemistry; Vol. 42, iss. 7
| Parent link: | New Journal of Chemistry Vol. 42, iss. 7.— 2018.— [P. 4959-4971] |
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| مؤلف مشترك: | |
| مؤلفون آخرون: | , , , , , , , , |
| الملخص: | Title screen The evaluation of N′-(pyridin-2-ylmethylene)nicotinohydrazide (HLI) and N,N′′′-bis(1-(pyridin-2-yl)-ethylidene)carbazide (H2LII) as linker precursors in the synthesis of novel PbII extended structures is described. An equimolar one-pot reaction of PbX2 (X = NO3−, CH3COO−) salts with HLI and H2LII in MeOH at 60 °C in a branched tube apparatus leads to heteroleptic complexes [Pb(HLI)(NO3)2]n (1), [Pb(LI)(CH3O)]n (2), [Pb2(H2LII)(NO3)4] (3) and [Pb2(HLII)(CH3COO)3]n (4), respectively. The nature of the anion in the parent PbII salt also influences the final structure. In all complexes, the PbII center exhibits a hemidirected coordination geometry with all the covalent bonds being concentrated on one hemisphere of the coordination sphere. The sterically available PbII ion participates in Pb⋯O/N tetrel bonding or Pb⋯Cg interaction as evidenced from the detailed structural and topological analysis of the described complexes. As a result of these interactions, the structures of all four compounds can be extended to a higher dimensional framework, which is further stabilized by hydrogen N-H⋯O/C-H⋯O and dihydrogen C-H⋯H-C bonds and/or π⋯π stacking interactions. The complementary Hirshfeld surface analysis of the discrete complex 3, considering covalent bonds, showed that the structure is highly dominated by H⋯X (X = O, H and C) and O⋯Y (Y = O, Pb, C and N) contacts, of which the O⋯Pb/H/N/C contacts are highly favoured. DFT based charge and energy decomposition (ETS-NOCV) calculations are performed in order to shed light on the nature of the non-covalent interactions that determine the stability of the obtained structures. Режим доступа: по договору с организацией-держателем ресурса |
| اللغة: | الإنجليزية |
| منشور في: |
2018
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| الموضوعات: | |
| الوصول للمادة أونلاين: | http://dx.doi.org/10.1039/C8NJ00525G |
| التنسيق: | الكتروني فصل الكتاب |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=657914 |
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| 200 | 1 | |a Extended lead(II) architectures engineered via tetrel bonding interactions |f G. Mahmoudi [et al.] | |
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| 300 | |a Title screen | ||
| 330 | |a The evaluation of N′-(pyridin-2-ylmethylene)nicotinohydrazide (HLI) and N,N′′′-bis(1-(pyridin-2-yl)-ethylidene)carbazide (H2LII) as linker precursors in the synthesis of novel PbII extended structures is described. An equimolar one-pot reaction of PbX2 (X = NO3−, CH3COO−) salts with HLI and H2LII in MeOH at 60 °C in a branched tube apparatus leads to heteroleptic complexes [Pb(HLI)(NO3)2]n (1), [Pb(LI)(CH3O)]n (2), [Pb2(H2LII)(NO3)4] (3) and [Pb2(HLII)(CH3COO)3]n (4), respectively. The nature of the anion in the parent PbII salt also influences the final structure. In all complexes, the PbII center exhibits a hemidirected coordination geometry with all the covalent bonds being concentrated on one hemisphere of the coordination sphere. The sterically available PbII ion participates in Pb⋯O/N tetrel bonding or Pb⋯Cg interaction as evidenced from the detailed structural and topological analysis of the described complexes. As a result of these interactions, the structures of all four compounds can be extended to a higher dimensional framework, which is further stabilized by hydrogen N-H⋯O/C-H⋯O and dihydrogen C-H⋯H-C bonds and/or π⋯π stacking interactions. The complementary Hirshfeld surface analysis of the discrete complex 3, considering covalent bonds, showed that the structure is highly dominated by H⋯X (X = O, H and C) and O⋯Y (Y = O, Pb, C and N) contacts, of which the O⋯Pb/H/N/C contacts are highly favoured. DFT based charge and energy decomposition (ETS-NOCV) calculations are performed in order to shed light on the nature of the non-covalent interactions that determine the stability of the obtained structures. | ||
| 333 | |a Режим доступа: по договору с организацией-держателем ресурса | ||
| 461 | |t New Journal of Chemistry | ||
| 463 | |t Vol. 42, iss. 7 |v [P. 4959-4971] |d 2018 | ||
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