[Sm(2,2'-thiobis(6-tert-butyl-4-methylphenolato))(2,6-di-tert-butyl phenolato)]2 | 442199-65-7

• 英文名称: [Sm(2,2'-thiobis(6-tert-butyl-4-methylphenolato))(2,6-di-tert-butyl phenolato)]2
• CAS: 442199-65-7
• 化学式: C₇₂H₉₈O₆S₂Sm₂
• 分子量: 1424.42
• InChiKey: KYTQXUSOYHIQQZ-UHFFFAOYSA-H

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为产物：
  描述：

  Sm(2,2'-thiobis(6-tert-butyl-4-methylphenolato))(2,6-di-tert-butyl phenolato)(tetrahydrofuran) 以 neat (no solvent) 为溶剂， 生成 [Sm(2,2'-thiobis(6-tert-butyl-4-methylphenolato))(2,6-di-tert-butyl phenolato)]2
  参考文献：
  名称：

  Symmetric and asymmetric samarium alkoxide derivatives of bridging sulfur biphenolate and binaphtholate ligands; synthetic, structural, and catalytic studies

  摘要：

  The new thio-binaphthol 2,2'thiobis(3,6-di-tert-butylnaphth-2-ol), and a phenolic analogue 2,2'thiobis(6-tert-butyl-4-methyl phen-2-ol) react with the Sm(III) aryloxide [Sm(OC6H3Bu2'-2,6)(3)] to give the first f-element complexes supported by S-bridged biphenolate or binaphtholate ancillary ligands, [Sm{1,1'-S(2-OC10H4Bu2'-3,6)(2)}(OC6H3Bu2'-2,6)](2) and [Sm{1,1'-S(2-OC6H2But-3-Me-5)(2)}(OC6H3Bu2t-2,6)](2). Symmetric and asymmetric derivatives of both ligands have been prepared by careful tuning of the preparative procedure, the asymmetric naphtholate derivative, and the ligand from which it derives have both been structurally characterised. The asymmetric derivatives are found to be highly selective catalysts for diol desymmetrisation. (C) 2002 Elsevier Science B.V. All rights reserved.

  DOI：

  10.1016/s0022-328x(01)01425-5