Synthesis beyond the redox-active tetrathiafulvalene (TTF) molecule: From a topological control in TTF based macrocycles, towards functional chemical systems

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Liens [1] http://okina.univ-angers.fr/marc.salle/publications [2] http://okina.univ-angers.fr/publications?f[author]=2775 [3] http://okina.univ-angers.fr/publications?f[author]=2681 [4] http://okina.univ-angers.fr/publications?f[author]=3073 [5] http://okina.univ-angers.fr/publications?f[author]=3114 [6] http://okina.univ-angers.fr/publications?f[author]=2825 [7] http://okina.univ-angers.fr/publications?f[author]=3116 [8] http://okina.univ-angers.fr/publications/ua2277

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Mechanical bonds and topological effects in radical dimer stabilization.

While mechanical bonding stabilizes tetrathiafulvalene (TTF) radical dimers, the question arises: what role does topology play in catenanes containing TTF units? Here, we report how topology, together with mechanical bonding, in isomeric [3]- and doubly interlocked [2]catenanes controls the formation of TTF radical dimers within their structural frameworks, including a ring-in-ring complex (for...

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Mechanically stabilized tetrathiafulvalene radical dimers.

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Computing Vertex PI Index of Tetrathiafulvalene Dendrimers

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تاریخ انتشار 2017