Trichloro-, mono-, di- and tri-organotin(IV) derivatives of hydridotris-(4-methylpyrazol-1-yl)borates

被引:33
作者
Lobbia, GG
Valle, G
Calogero, S
Cecchi, P
Santini, C
Marchetti, F
机构
[1] CNR,CTR RIC BIOPOLIMERI,I-35100 PADUA,ITALY
[2] UNIV VENICE,DIPARTIMENTO CHIM FIS,I-30123 VENICE,ITALY
[3] UNIV TUSCIA,DIPARTIMENTO AGROBIOL & AGROCHIM,I-01100 VITERBO,ITALY
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 1996年 / 12期
关键词
D O I
10.1039/dt9960002475
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Tin(IV) complexes of general formula SnR(n)Cl(3-n)[HB(mpz)(3)] (R = Me or Ph; n = 0-2; mpz = 4-methylpyrazolyl) have been synthesised and characterised by IR, far-IR, H-1, C-13, Sn-119 NMR and; Sn-119 Mossbauer spectroscopy. Their. stability towards self-decomposition decreases with increasing number of Sn-bonded aryl or alkyl groups. In addition, triorganotin(rv) complexes of the same ligand as well as of [HB(pz)(3)](-) and [HB(dmpz)(3)] (pz = pyrazolyl, dmpz = 3,5-dimethylpyrazolyl) have been synthesised and characterised by IR and NMR techniques but,due to their low stability (even in the solid state), could not be characterised by Mossbauer spectroscopy. Both the crystal structures of SnCl3 [HB(mpz)(3)] and SnPhCl(2) [HB(mpz)(3)] show the tin atom in a skewed octahedral environment. The structure-of the deboronated adduct SnMe(2)Cl(2)(Hmpz)(2), obtained from attempted recrystallisation of SnMe(2)Cl[HB(mpz)(3)], in which the Cl, the Me and the N-donors are in the all-trans configuration, has been determined.
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页码:2475 / 2483
页数:9
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