2014
DOI: 10.1002/ange.201310975
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C4 Cumulene and the Corresponding Air‐Stable Radical Cation and Dication

Abstract: A neutral C 4 cumulene 1 that includes a cyclic alkyl(amino) carbene (cAAC), its air-stable radical cation 1C + , and dication 1 2+ have been synthesized. The redox property of 1C + was studied by cyclic voltammetry. EPR and theoretical calculations show that the unpaired electron in 1C + is mainly delocalized over the central C 4 backbone. The commercially available CBr 4 is utilized as a source of dicarbon in the cumulene synthesis.

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Cited by 61 publications
(47 citation statements)
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References 45 publications
(25 reference statements)
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“…These ligands are stronger π acceptors than NHCs . Moreover, the syntheses of [3]cumulenes with CAACs as terminal groups have been successful, contrary to NHCs . The PESs of CAAC [2 n ]cumulenes are also shallower than those of the odd cumulenes, but the two sets are more similar than in the case of the NHC cumulenes (Figure b).…”
Section: Resultsmentioning
confidence: 98%
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“…These ligands are stronger π acceptors than NHCs . Moreover, the syntheses of [3]cumulenes with CAACs as terminal groups have been successful, contrary to NHCs . The PESs of CAAC [2 n ]cumulenes are also shallower than those of the odd cumulenes, but the two sets are more similar than in the case of the NHC cumulenes (Figure b).…”
Section: Resultsmentioning
confidence: 98%
“…For example, they can be used as molecular wires as their conductivity is significantly better than the other possible form of linear carbon chains, polyynes . Strong σ donors as end‐capping groups of the cumulene chain give their radical species a remarkable stability, with some of these radicals stable even to air . Cumulenes have been known for around 100 years, however, [3]cumulenes that have strong σ donors as terminal groups, such as N‐heterocyclic or cyclic (alkyl)(amino) carbenes (NHCs or CAACs, respectively), have only recently been studied .…”
Section: Introductionmentioning
confidence: 99%
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“…[15] While the CAAC ligands in this neutral compound are expectedly co-planar, when twice-oxidized to a dication (3 2+ ), which is isoelectronic with 2, the ligands remain essentially eclipsed rather than adopting a staggered conformation. [15] While the CAAC ligands in this neutral compound are expectedly co-planar, when twice-oxidized to a dication (3 2+ ), which is isoelectronic with 2, the ligands remain essentially eclipsed rather than adopting a staggered conformation.…”
Section: Methodsmentioning
confidence: 95%
“…4.07 ) ist die sterische Abstoßung in 2 geringer. [15] Das UV/Vis-Spektrum von 2 zeigt eine intensive Bande bei 382 nm (Abbildung 3). Eine zeitabhängige (TD-)DFTAnalyse sagt ein solches Spektrum als Überlagerung von drei Übergängen bei l = 353, 366 und 380 nm voraus.…”
Section: +unclassified