2008
DOI: 10.1107/s1600536808004893
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1,3-Bis(3-phenylpropyl)-1H-benzimidazole-2(3H)-tellurone

Abstract: The title compound, C25H26N2Te, was synthesized from bis­[1,3-bis­(3-phenyl­prop­yl)benzimidazolidin-2-yl­idene] and Te in a toluene solution. The molecule possesses a twofold rotation axis passing through the Te atom and the center of the benzimidazole ring system. The benzimidazole ring system makes an angle of 67.9 (4)° with the phenyl rings.

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Cited by 6 publications
(2 citation statements)
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“…Chart assembles a few other potential Te-donor ligands, which did not yet find successful application in coordination chemistry. 719 was prepared from the corresponding NHC dimer by treatment with tellurium, which resembles the protocol developed by Lappert (vide supra) and related unsymmetric benzimidazolin-2-tellone derivatives such as 721a and 721b were prepared in a similar fashion .…”
Section: N-heterocyclic Carbene Adducts Of Group 16 Elementsmentioning
confidence: 99%
“…Chart assembles a few other potential Te-donor ligands, which did not yet find successful application in coordination chemistry. 719 was prepared from the corresponding NHC dimer by treatment with tellurium, which resembles the protocol developed by Lappert (vide supra) and related unsymmetric benzimidazolin-2-tellone derivatives such as 721a and 721b were prepared in a similar fashion .…”
Section: N-heterocyclic Carbene Adducts Of Group 16 Elementsmentioning
confidence: 99%
“…NHCs are frequently observed in work areas such as the synthesis of organic or organometallic catalysts, bioactive materials, and metal-organic framework preparation. [7,[8][9][10][11][12][13] The synthesis of NHCs is generally carried out in two pathways. The first method is the deprotonation of azolium salts in the presence of a strong base, and the second method is the reduction of urea derivatives.…”
Section: Introductionmentioning
confidence: 99%