2018
DOI: 10.1039/c8ce00413g
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X4TCNQ2− dianions: versatile building blocks for supramolecular systems

Abstract: A new synthetic approach has led to the incorporation of TCNQ and F4TCNQ dianions into a wide variety of structures.

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Cited by 21 publications
(31 citation statements)
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“…Unfortunately, no crystals suitable for X‐Ray Diffraction structural analysis were generated for either the TCNQF 1− or TCNQF 2− derivatives. Indeed, the entire two‐electron reduced TCNQF n 2− field of metal complexes is almost devoid of X‐ray structural data unless other ligands in addition to TNCQF 4 2− are coordinated to the metal and even structures of metal complexes solely containing TCNQF n 1− as a ligand are rare.…”
Section: Resultssupporting
confidence: 78%
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“…Unfortunately, no crystals suitable for X‐Ray Diffraction structural analysis were generated for either the TCNQF 1− or TCNQF 2− derivatives. Indeed, the entire two‐electron reduced TCNQF n 2− field of metal complexes is almost devoid of X‐ray structural data unless other ligands in addition to TNCQF 4 2− are coordinated to the metal and even structures of metal complexes solely containing TCNQF n 1− as a ligand are rare.…”
Section: Resultssupporting
confidence: 78%
“…However, the two‐electron reduced TCNQ 2− compounds are highly air‐sensitive . Such materials, in principle provide novel framework structures and can be stable when additional nitrogen based donors are also present, as reviewed by Abrahams in a recent survey of the field. Another method of enhancing stability is the use of the fluoride derivative, TCNQF 4 , in the chemical synthesis.…”
Section: Introductionmentioning
confidence: 93%
“…Schematic illustration of the two-step fabrication procedure of a metal oxide@open-tubular N-doped carbon column (MO x @OTNCC) electrocatalyst for OER. The structure of M@TCNQ (with a formula of M­[TCNQ] 2 ) was drawn as inspired from the work of Abrahams et al …”
Section: Introductionmentioning
confidence: 99%
“…Achievement of such advanced properties requires, however, an expansion of the library of easily accessible and electroactive molecules with relatively stable radical forms. The most commonly studied radicals comprise α-diimines [12], dithiolenes [13][14][15], oxolenes [16,17], nitronyl nitroxides [18,19], tetrathiafulvalene (TTF) derivatives [20], π-conjugated macrocycles [21], TCNE and TCNQ derivatives [22][23][24][25], and verdazyl radicals [26].…”
Section: Introductionmentioning
confidence: 99%