2001
DOI: 10.1002/1521-3749(200103)627:3<458::aid-zaac458>3.0.co;2-n
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Abstract: The syntheses of the asymmetrically substituted tetraorganodistannoxanes [t-Bu 2 (X)SnOSn(Y)(CH 2 SiMe 3 ) 2 ] 2 (1, X = Y = OH; 2, X = Cl, Y = OH; 3, X = Y = Cl) are reported and their structures in solution and in the solid state are characterized by multinuclear NMR spectroscopy and single crystal X-ray analyses. In toluene, the tetrahydroxysubstituted derivative 1 is in equilibrium with the organotin oxides cyclo-[t-Bu 2 Sn{OSn(CH 2 SiMe 3 ) 2 } 2 O] (4), cyclo-[(Me 3 SiCH 2 ) 2 Sn(OSnt-Bu 2 ) 2 O] (5), an… Show more

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Cited by 32 publications
(36 citation statements)
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“…The reason for selective formation of the mer-isomer under these reaction conditions is still not understood. [14] The reaction of mer-[(Bu 3 SnO) 3 Te(OH) 3 ] (1) with two equivalents of (Ph 2 SnOH) 2 CH 2 [15] gave, with elimination of water and one equivalent of tributyltin hydroxide (Bu 3 SnOH), the spirocyclic tellurastannoxane derivative trans-[(Bu 3 SnO) 2 {CH 2 (Ph 2 SnO) 2 } 2 Te] (2) in good yields [Equation (2)]. [13] The identity of these species was unambiguously proven by 119 Sn and 125 Te NMR spectroscopy, although all attempts to isolate pure compounds from the mixtures failed.…”
Section: Resultsmentioning
confidence: 99%
“…The reason for selective formation of the mer-isomer under these reaction conditions is still not understood. [14] The reaction of mer-[(Bu 3 SnO) 3 Te(OH) 3 ] (1) with two equivalents of (Ph 2 SnOH) 2 CH 2 [15] gave, with elimination of water and one equivalent of tributyltin hydroxide (Bu 3 SnOH), the spirocyclic tellurastannoxane derivative trans-[(Bu 3 SnO) 2 {CH 2 (Ph 2 SnO) 2 } 2 Te] (2) in good yields [Equation (2)]. [13] The identity of these species was unambiguously proven by 119 Sn and 125 Te NMR spectroscopy, although all attempts to isolate pure compounds from the mixtures failed.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, reactions between Te(OH) 6 and other triorganotin methoxides, R 3 SnOMe (R ϭ Me, cHex, Ph), also provided mixtures of products that could not be purified. [14] The reaction of mer-[(Bu 3 SnO) 3 Te(OH) 3 ] (1) with two equivalents of (Ph 2 SnOH) 2 CH 2 [15] gave, with elimination of water and one equivalent of tributyltin hydroxide (Bu 3 SnOH), the spirocyclic tellurastannoxane derivative trans-[(Bu 3 SnO) 2 {CH 2 (Ph 2 SnO) 2 } 2 Te] (2) in good yields [Equation (2)]. (2) Compound 2 is a colorless crystalline material.…”
Section: Resultsmentioning
confidence: 99%
“…These belong to the well-known family of ladder structures, which consist of a central distannoxane (Sn 2 O 2 ) motif. 17 All the tin atoms in both of these com-pounds are present in a distorted trigonal bipyramidal geometry. The equatorial sites are occupied by two carbon atoms and one oxygen atom.…”
Section: Scheme 3 Synthesis Of Tetraorganodistannoxane Laddersmentioning
confidence: 99%