diphenoxydi(pyrrolidin-1-yl)palladium | 144270-18-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: diphenoxydi(pyrrolidin-1-yl)palladium
• CAS: 144270-18-8
• 化学式: C₂₀H₂₈N₂O₂Pd
• 分子量: 434.875
• InChiKey: NZTIHAFXKWLWFJ-UHFFFAOYSA-L

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

• 作为反应物：
  描述：

  diphenoxydi(pyrrolidin-1-yl)palladium 在 phenol 作用下， 以 二氯甲烷 、 正戊烷 为溶剂， 以82%的产率得到trans-{Pd(OPh)2(pyrrolidine)2*2HOPh}
  参考文献：
  名称：

  钯和铂二苯醚氧化物和芳基苯酚氧化物与胺供体的配合物：氢键对结构和性能的影响

  摘要：

  Several palladium and platinum phenoxides, [Pd(OPh)2L2] (L2 = tmeda (1), (pyrrolidine)2 (2), (N-methylpyrrolidine)2 (3)) and [M(OPh)(NCN)] (NCN = C6H3{CH2NMe2}2-2,6); M = Pd (5), Pt (6)) have been synthesized and characterized with special emphasis on the role of both N-H-0 and 0-H-0 hydrogen bonding in the resulting structures of these metal phenoxides. The [Pd(OPh)2L2] (1-3) complexes were obtained from the reaction of Pd(OAc)2 with 2 equiv of sodium phenoxide in the presence of the neutral ligand. The terdentate N-C-N-bound arylmetal complexes, [M(OPh)(NCN)], 5 and 6, were synthesized by reacting [M(C6H3{CH2NMe2}2-2,6)(H2O)]BF4 With sodium phenoxide. Both 2,5, and 6 react with excess phenol to form the corresponding phenol adducts, 4, 7, and 8, respectively. The structures of the phenoxides 2 and 5 and the phenol adducts 4 and 7 were studied by X-ray diffraction methods to establish their stereochemistry as well as the nature and structural details of the hydrogen bonding in the phenol adducts. Crystals of trans-[Pd(OPh)2(Pyrrolidine)2] (2) are tetragonal with a = b = 18.6615 (15) angstrom, c = 10.7713 (6) angstrom, space group I4(1)/a, Z = 8, and R = 0.026 for 1774 reflections with I greater-than-or-equal-to 2.5sigma(I); crystals of trans-[Pd-(OPh)2(pyrrolidine)2]-HOPh (4) are monoclinic with a = 6.4039 (3) angstrom, b = 15.497 (1) angstrom, c = 15.085 (1) angstrom, beta = 99.832 (4)-degrees, space group P2(1)/c, Z = 2, and R = 0.032 for 2224 reflections with I greater-than-or-equal-to 2.5sigma(I); crystals of [Pd(OPh)(C6H3{CH2NMe2}2-2,6)] (5) are monoclinic with a = 6.1490 (2) angstrom, b = 12.0595 (6) angstrom, c = 23.1829 (10) angstrom, beta = 97.251 (3)-degrees, space group P2(1)/c, Z = 4, and R = 0.0223 for 3387 reflections with I greater-than-or-equal-to 2.5sigma(I); and crystals of [Pd(OPh)(C6H3{CH2NMe2}2-2,6)]-HOPh (7) are monoclinic with a = 8.5400 (5) angstrom, b = 12.0445 (7) angstrom, c = 22.4473 (14) angstrom, beta = 100.779 (5)-degrees, space group P2(1)/n, Z = 4, and R = 0.0428 for 3081 reflections with I greater-than-or-equal-to 2.5sigma(I). Palladium phenoxide 2 has a unique dimeric structure consisting of two trans-Pd-(OPh)2(pyrrolidine)2 monomers being held together by four identical (pyrrolictine)N-H ... 0(phenoxide) hydrogen bonds (N...O = 2.866 (3) angstrom). The Pd atoms are in close proximity of each other, but the resulting Pd ... Pd distance (3.0960 (3) angstrom) points to some repulsion between the metal centers. In the corresponding phenol adduct, 4, the dimeric structure is broken down by interaction of two phenol molecules resulting in two (phenol)O-H...O(phenoxide) hydrogen bonds (2.638 (4) angstrom). The structural features of the NCN-bound palladium phenoxides, 5 and 7, reflect the effect of changing the trans ligand from phenoxide to aryl on the Pd-phenoxide bonding. In 5 a very short (phenoxide)C-O bond of 1.305 (3) angstrom is observed which lengthens to 1.330 (6) angstrom in the phenol adduct 7. The strong hydrogen bonding in 7 is indicated by the short (phenoxide)O ... 0 (phenol) bond distance of 2.567 (6) angstrom (cf. 2.638 (4) angstrom in 4). These results have been used to synthesize new monodentate N-C-N-metal catecholate complexes, [M(C6H3{CH2NMe2}2-2,6)-(OC6H4OH-2)] (9 (M = Pd), 10 (M = Pt)), which contain an intramolecular O-H...O hydrogen bond. H-1 NMR studies show that 2 is monomeric in solution.Exchange between coordinated phenoxide and associated phenol in 4 remains slow on the NMR time scale (up to 97-degrees-C) but occurs on the laboratory time scale (experiments with pentadeuteriophenol). The arylpalladium phenoxide complex 7 undergoes fast exchange between phenoxide and associated phenol indicating the large trans effect of the aryl ligand (cf. long Pd-O bond in 5). This exchange is slow on the H-1 NMR time scale in the corresponding platinum complex 8. Similarly, intramolecular phenol/phenoxide exchange is fast on the H-1 NMR time scale in the Pd-catecholate 9 but slow in the Pt-catecholate 10. Thermodynamic parameters for the association of phenol with the palladium diphenoxide complexes 2 and 3 have been determined by means of H-1 NMR spectroscopy.

  DOI：

  10.1021/om00060a032
• 作为产物：
  描述：

  四氢吡咯 、 sodium phenoxide 、 palladium diacetate 以 甲醇 、 二氯甲烷 为溶剂， 以89%的产率得到diphenoxydi(pyrrolidin-1-yl)palladium
  参考文献：
  名称：

  钯和铂二苯醚氧化物和芳基苯酚氧化物与胺供体的配合物：氢键对结构和性能的影响

  摘要：

  Several palladium and platinum phenoxides, [Pd(OPh)2L2] (L2 = tmeda (1), (pyrrolidine)2 (2), (N-methylpyrrolidine)2 (3)) and [M(OPh)(NCN)] (NCN = C6H3{CH2NMe2}2-2,6); M = Pd (5), Pt (6)) have been synthesized and characterized with special emphasis on the role of both N-H-0 and 0-H-0 hydrogen bonding in the resulting structures of these metal phenoxides. The [Pd(OPh)2L2] (1-3) complexes were obtained from the reaction of Pd(OAc)2 with 2 equiv of sodium phenoxide in the presence of the neutral ligand. The terdentate N-C-N-bound arylmetal complexes, [M(OPh)(NCN)], 5 and 6, were synthesized by reacting [M(C6H3{CH2NMe2}2-2,6)(H2O)]BF4 With sodium phenoxide. Both 2,5, and 6 react with excess phenol to form the corresponding phenol adducts, 4, 7, and 8, respectively. The structures of the phenoxides 2 and 5 and the phenol adducts 4 and 7 were studied by X-ray diffraction methods to establish their stereochemistry as well as the nature and structural details of the hydrogen bonding in the phenol adducts. Crystals of trans-[Pd(OPh)2(Pyrrolidine)2] (2) are tetragonal with a = b = 18.6615 (15) angstrom, c = 10.7713 (6) angstrom, space group I4(1)/a, Z = 8, and R = 0.026 for 1774 reflections with I greater-than-or-equal-to 2.5sigma(I); crystals of trans-[Pd-(OPh)2(pyrrolidine)2]-HOPh (4) are monoclinic with a = 6.4039 (3) angstrom, b = 15.497 (1) angstrom, c = 15.085 (1) angstrom, beta = 99.832 (4)-degrees, space group P2(1)/c, Z = 2, and R = 0.032 for 2224 reflections with I greater-than-or-equal-to 2.5sigma(I); crystals of [Pd(OPh)(C6H3{CH2NMe2}2-2,6)] (5) are monoclinic with a = 6.1490 (2) angstrom, b = 12.0595 (6) angstrom, c = 23.1829 (10) angstrom, beta = 97.251 (3)-degrees, space group P2(1)/c, Z = 4, and R = 0.0223 for 3387 reflections with I greater-than-or-equal-to 2.5sigma(I); and crystals of [Pd(OPh)(C6H3{CH2NMe2}2-2,6)]-HOPh (7) are monoclinic with a = 8.5400 (5) angstrom, b = 12.0445 (7) angstrom, c = 22.4473 (14) angstrom, beta = 100.779 (5)-degrees, space group P2(1)/n, Z = 4, and R = 0.0428 for 3081 reflections with I greater-than-or-equal-to 2.5sigma(I). Palladium phenoxide 2 has a unique dimeric structure consisting of two trans-Pd-(OPh)2(pyrrolidine)2 monomers being held together by four identical (pyrrolictine)N-H ... 0(phenoxide) hydrogen bonds (N...O = 2.866 (3) angstrom). The Pd atoms are in close proximity of each other, but the resulting Pd ... Pd distance (3.0960 (3) angstrom) points to some repulsion between the metal centers. In the corresponding phenol adduct, 4, the dimeric structure is broken down by interaction of two phenol molecules resulting in two (phenol)O-H...O(phenoxide) hydrogen bonds (2.638 (4) angstrom). The structural features of the NCN-bound palladium phenoxides, 5 and 7, reflect the effect of changing the trans ligand from phenoxide to aryl on the Pd-phenoxide bonding. In 5 a very short (phenoxide)C-O bond of 1.305 (3) angstrom is observed which lengthens to 1.330 (6) angstrom in the phenol adduct 7. The strong hydrogen bonding in 7 is indicated by the short (phenoxide)O ... 0 (phenol) bond distance of 2.567 (6) angstrom (cf. 2.638 (4) angstrom in 4). These results have been used to synthesize new monodentate N-C-N-metal catecholate complexes, [M(C6H3{CH2NMe2}2-2,6)-(OC6H4OH-2)] (9 (M = Pd), 10 (M = Pt)), which contain an intramolecular O-H...O hydrogen bond. H-1 NMR studies show that 2 is monomeric in solution.Exchange between coordinated phenoxide and associated phenol in 4 remains slow on the NMR time scale (up to 97-degrees-C) but occurs on the laboratory time scale (experiments with pentadeuteriophenol). The arylpalladium phenoxide complex 7 undergoes fast exchange between phenoxide and associated phenol indicating the large trans effect of the aryl ligand (cf. long Pd-O bond in 5). This exchange is slow on the H-1 NMR time scale in the corresponding platinum complex 8. Similarly, intramolecular phenol/phenoxide exchange is fast on the H-1 NMR time scale in the Pd-catecholate 9 but slow in the Pt-catecholate 10. Thermodynamic parameters for the association of phenol with the palladium diphenoxide complexes 2 and 3 have been determined by means of H-1 NMR spectroscopy.

  DOI：

  10.1021/om00060a032