“…This result corresponds to the structure of BbtTeF 2 TeBbt:13 Sterically protected tellurenyl fluorides are stable in the dimerized molecular form RTeF 2 TeR. This structure type was first described for tellurenyl chlorides and bromides,11, 30a but in the meantime has also been found for iodides 30b…”
Section: Se 125te and 19f Nmr Data [Ppm Hz] Of The Se‐f And Te‐fsupporting
Joining the stable: The first examples of the highly instable selenenyl fluorides RSeF are prepared from the reaction on the tin selenide RSeSnMe(3) with XeF(2). Through the use of extremely large protecting groups (m-terphenyl ligands) which stabilizes the RSeF units against disproportionation, the compounds could be isolated and characterized by NMR spectroscopy and single-crystal structure analysis (see structure).
“…This result corresponds to the structure of BbtTeF 2 TeBbt:13 Sterically protected tellurenyl fluorides are stable in the dimerized molecular form RTeF 2 TeR. This structure type was first described for tellurenyl chlorides and bromides,11, 30a but in the meantime has also been found for iodides 30b…”
Section: Se 125te and 19f Nmr Data [Ppm Hz] Of The Se‐f And Te‐fsupporting
Joining the stable: The first examples of the highly instable selenenyl fluorides RSeF are prepared from the reaction on the tin selenide RSeSnMe(3) with XeF(2). Through the use of extremely large protecting groups (m-terphenyl ligands) which stabilizes the RSeF units against disproportionation, the compounds could be isolated and characterized by NMR spectroscopy and single-crystal structure analysis (see structure).
“…In a nice illustration of how an inorganic element can dictate molecular structure, bis(pentafluorophenyl)tellurium oxide, [(F 5 C 6 ) 2 Te(μ-O)] 2 ( 948 ), is a centrosymmetric dimer with a planar Te 2 O 2 ring, while its selenium congener is a weakly associated hexamer, [(F 5 C 6 ) 2 SeO] 6 ( 949 ), with long Se---O and Se---Se bonds; both species were formed via the oxidation of the Se(II) and Te(II) precursors, Ch(C 6 F 5 ) 2 (Ch = Se and Te), with m -chloroperbenzoic acid in chloroform . Structurally related tellurium oxide heterocycles characterized in the literature include a polymorph of 948 , [(2,4,6-Ph 3 C 6 H 2 )Te(μ-O)X] 2 (X = Br and I; 950 and 951 ), the siloxy-capped tellurium(VI) oxide [(Me 3 SiO) 4 Te(μ-O)] 2 ( 952 ), [(2,6-(MeO) 2 C 6 H 3 )Te(μ-O)OMe] 2 ( 953 ), salts of the dianion [F 3 Te(μ-O)TeF 3 ] 2– ( 954 ), and the ureatotellurium oxide [( t BuNC(O)N t Bu)Te(μ-O)] 2 ( 955 ) …”
Section: Inorganic
Rings Derived From Group 12–17
Elementsmentioning
“…Only the tellurium atom meets these criteria, and in each of them, the Te atom is involved in unusual TeÁ Á ÁX (X = F, Cl, Br, and I) interactions. Among these thirteen systems, two contain fluorine, 19,20 five chlorine, [21][22][23][24][25] two bromine, 23,26 and four iodine 23,27,28 atoms as ligands (Fig. S1, ESI †).…”
In a crystal, a pair of homoanions (Te(C5H5)Cl4-) are arranged in a parallel manner, close enough to interact with each other. Quantum chemical analysis indicates the existence of two strong...
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