2020
DOI: 10.1016/j.jorganchem.2020.121344
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Dinuclear organotin compounds carrying naphthylene- and biphenylene-spacer groups

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Cited by 2 publications
(1 citation statement)
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“…[24,59,[65][66] Interconnection of such organotin tectons through di-or oligotopic ligands such as carboxylates, dithiocarbamates, phosphates, etc., constitutes a pathway to a plethora of metalla-supramolecular assemblies. [65][66] In continuation of previous works, [11,24,59,[65][66][67] herein we report on the formation of two di-nuclear organotin compounds carrying voluminous organic substituents at the metal atoms that were then functionalized with a SnÀ X bond (X = Cl, I). In addition, the potential for the formation of a novel class of tetra-nuclear macrocyclic structures through linkage of the halogenated building blocks by SnÀ OÀ Sn fusion [11,68] was explored.…”
Section: Introductionmentioning
confidence: 54%
“…[24,59,[65][66] Interconnection of such organotin tectons through di-or oligotopic ligands such as carboxylates, dithiocarbamates, phosphates, etc., constitutes a pathway to a plethora of metalla-supramolecular assemblies. [65][66] In continuation of previous works, [11,24,59,[65][66][67] herein we report on the formation of two di-nuclear organotin compounds carrying voluminous organic substituents at the metal atoms that were then functionalized with a SnÀ X bond (X = Cl, I). In addition, the potential for the formation of a novel class of tetra-nuclear macrocyclic structures through linkage of the halogenated building blocks by SnÀ OÀ Sn fusion [11,68] was explored.…”
Section: Introductionmentioning
confidence: 54%