2-Triphenylstannylmercapto-pyridin | 20637-89-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 2-Triphenylstannylmercapto-pyridin
• 英文别名: Triphenyl-(2-thiopyridonyl)-zinn；Ph3SnS(2-C5H4N)；pyridin2-2-thiolate-triphenyltin；Agn-PC-0lsexu；pyridine-2-thiolate;triphenylstannanylium
• CAS: 20637-89-2
• 化学式: C₂₃H₁₉NSSn
• 分子量: 460.187
• InChiKey: BIEQTCUAVSGELN-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  3.84
• 重原子数：
  26
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  38.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-Triphenylstannylmercapto-pyridin 、 copper(l) chloride 以 四氢呋喃 为溶剂， 以70%的产率得到三苯基氯化锡
  参考文献：
  名称：

  Mercapto derivatives of triorganotin Y,C,Y-pincer complexes: Role of Y,C,Y-chelating ligands in a new coordination mode of organotin compounds

  摘要：

  We report the use of triorganotin fragments R2L1-2ST, containing N,C,N and O,C,O-Iigands L1-2 (L-1 = C6H3(Me2NCH2)(2)-2,6(-), L-2 = C6H3 ((BuOCH2)-Bu-l)(2)-2,6(-)) on stabilization of both thiol-form in R2L1-2 Sn-2-SPy (2-SPy = pyridine-2-thiolate) and thione-form in R2L1-2 Sn(mimt) (mimt = 1-methylimidazole-2-thiolate) of the polar groups. Treatment of ionic organotin compounds [(Me2LSn)-Sn-1](+)[Cl](-)(1) and [Ph2L2 Sn](+)[OTf](-) (2) with appropriate sodium salts Na-2-SPy and Na(mimt) resulted in the isolation of (Me2LSn)-Sn-1-2-SPy (3), Ph2L2 Sn-2-SPy (4), (Me2LSn)-Sn-1(mimt) (5), (Ph2LSn)-Sn-2(mimt) (6). While polar group 2-SPy exists in its thiol-tautomeric form in compounds 3 and 4, the second polar group (mimt) has been stabilized as the thione-tautomeric form by triorganotin fragments R2L1-2 Sn in compounds 5 and 6. The products were characterized by H-1, C-13 and Sn-119 NMR and IR spectroscopy, ESI/MS, elemental analyses and structures of 3, 6 were determined by X-ray diffraction study. The reactivity of compound 4 containing non-coordinated nitrogen atom of 2-SPy polar group towards CuCl and AgNO3 is also reported. The reactions led to isolation of organotin compounds Ph2L2 SnCl (7) and Ph2L2 SnNO3 (8) as the result of polar group transfer. The mechanism of this reaction has been investigated and compounds Ph3Sn-2-SPy (9) and Ph2L2 Sn-4-SPy (10) (4-SPy = pyridine-4-thic late) have been prepared for this purpose. (c) 2007 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jorganchem.2007.04.006

文献信息

• Synthesis of new heterometallic complexes by tin–sulfur bond cleavage of pySSnPh3 (pySH = pyridine-2-thiol) at triruthenium and triosmium centres
  作者：Arun K. Raha、Shishir Ghosh、Iqbal Hossain、Shariff E. Kabir、Brian K. Nicholson、Graeme Hogarth、Luca Salassa

  DOI：10.1016/j.jorganchem.2010.11.022

  日期：2011.5

  complex, [Ru2(CO)4(SnPh3)2(μ-pyS)2] (1), the main product of the oxidative-addition of pySSnPh3 to Ru3(CO)12 in refluxing benzene, is [Ru(CO)2(pyS)(SnPh3)] synthon. It reacts with PPh3 to give [Ru(CO)2(SnPh3)(PPh3)(κ2-pyS)] (2) and further with Ru3(CO)12 or [Os3(CO)10(NCMe)2] to afford the butterfly clusters [MRu3(CO)12(SnPh3)(μ3-pyS)] (3, M=Ru; 4, M=Os). Direct addition of pySSnPh3 to [Os3(CO)10(NCMe)2]

  钌-锡络合物[Ru 2（CO）4（SnPh 3）2（μ-pyS）2 ]（1），是在回流的苯中将pySSnPh 3氧化成Ru 3（CO）12的主要产物，是[Ru（CO）2（pyS）（SnPh 3）]合成子。其与反应PPH 3得到的[Ru（CO）2（SnPh 3）（PPH 3）（κ 2 -pyS）]（2），并进一步用孺3（CO）12或[O的3（CO）10（NCMe ）2 ]，得到蝴蝶簇[MRU 3（CO）12（SnPh 3）（μ 3 -pyS）]（3，M =茹; 4，M = OS）。直接加入pySSnPh的3至[O的3（CO）10（NCMe）2 ]在70℃下给出了[Os 3（CO）9（SnPh 3）（μ 3 -pyS）]（5）作为唯一的双金属化合物，而具有不饱和了[Os 3（CO）8 μ 3 -PPh 2 CH 2 P（博士）C 6 H ^ 4}（μ-H）]先前报告的[Os 3（CO）8（μ
• Mercapto derivatives of triorganotin Y,C,Y-pincer complexes: Role of Y,C,Y-chelating ligands in a new coordination mode of organotin compounds
  作者：Jana Martincová、Libor Dostál、Jan Taraba、Aleš Růžička、Roman Jambor

  DOI：10.1016/j.jorganchem.2007.04.006

  日期：2007.7

  We report the use of triorganotin fragments R2L1-2ST, containing N,C,N and O,C,O-Iigands L1-2 (L-1 = C6H3(Me2NCH2)(2)-2,6(-), L-2 = C6H3 ((BuOCH2)-Bu-l)(2)-2,6(-)) on stabilization of both thiol-form in R2L1-2 Sn-2-SPy (2-SPy = pyridine-2-thiolate) and thione-form in R2L1-2 Sn(mimt) (mimt = 1-methylimidazole-2-thiolate) of the polar groups. Treatment of ionic organotin compounds [(Me2LSn)-Sn-1](+)[Cl](-)(1) and [Ph2L2 Sn](+)[OTf](-) (2) with appropriate sodium salts Na-2-SPy and Na(mimt) resulted in the isolation of (Me2LSn)-Sn-1-2-SPy (3), Ph2L2 Sn-2-SPy (4), (Me2LSn)-Sn-1(mimt) (5), (Ph2LSn)-Sn-2(mimt) (6). While polar group 2-SPy exists in its thiol-tautomeric form in compounds 3 and 4, the second polar group (mimt) has been stabilized as the thione-tautomeric form by triorganotin fragments R2L1-2 Sn in compounds 5 and 6. The products were characterized by H-1, C-13 and Sn-119 NMR and IR spectroscopy, ESI/MS, elemental analyses and structures of 3, 6 were determined by X-ray diffraction study. The reactivity of compound 4 containing non-coordinated nitrogen atom of 2-SPy polar group towards CuCl and AgNO3 is also reported. The reactions led to isolation of organotin compounds Ph2L2 SnCl (7) and Ph2L2 SnNO3 (8) as the result of polar group transfer. The mechanism of this reaction has been investigated and compounds Ph3Sn-2-SPy (9) and Ph2L2 Sn-4-SPy (10) (4-SPy = pyridine-4-thic late) have been prepared for this purpose. (c) 2007 Elsevier B.V. All rights reserved.