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Embracing ligands. A synthetic strategy towards new nitrogen-thioether multidentate ligands and characterization of the cobalt(III) complexes

机译:拥抱配体。一种新的氮-硫醚多齿配体的合成策略和钴(III)配合物的表征

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摘要

The synthesis of the hexadentate ligand 2,2,9,9-tetra(methyleneamine)-4,7-dithiadecane (EtN(4)S(2)amp) is reported. The ligand is of a type in which bifurcations of the chain occur at atoms other than donor atoms. The cobalt(III) complex [Co(EtN(4)S(2)amp)](3+) (1) was isolated and characterized. The synthetic methodology also results in a number of by-products, notably 2,9,9-tris(methyleneamine)-9-methylenehydroxy-4,7-dithiadecane (Et(HO)N(3)S(2)amp) and an eleven-membered pendant arm macrocyclic ligand 6,10-dimethyl-6,10-bis(methyleneamine)-1,4-dithia-8-azaacycloundec-7- ene (dmatue). The complexes [Co(Et(HO)N(3)S(2)amp)](3+) (2), in which the alcohol is coordinated to the metal ion, and [Co(dmatue)Cl](2+) (4) were isolated and characterized. Et(HO)N(3)S(2)amp also undergoes complexation with cobalt(III) to produce two isomers endo-[Co(Et(HO) N(3)S(2)amp)Cl](2+) (endo-3) and exo-[Co(Et(HO) N(3)S(2)amp)Cl](2+) (exo-3), both with an uncoordinated alcohol group. endo- 3 has the alcohol positioned cis, and exo-3 trans, to the sixth metal coordination site. Reaction of 1 with isobutyraldehyde, paraformaldehyde and base in dimethylformamide results in the encapsulated complex [Co(1,5,5,9,13,13-hexamethyl-18,21-dithia-3,7,11,15-tetraazabicyclo[7.7.6]docosa- 3,14-diene)](ClO4)(3) . 2H(2)O ([Co(Me(6)docosadieneN(4)S(2))](3+) ( 5). All complexes have been characterized by single crystal X-ray study. The low-temperature (11 K) absorption spectrum of 1 has been measured in Nafion films with spin-allowed (1)A(1g) --> T-1(1g) and (1)A(1g) --> T-1(2g) and spin forbidden (1)A(1g) --> T-3(1g) and (1)A(1g) --> T-3(2g) bands observed. The octahedral ligand-field parameters were determined (10Dq = 22570 cm(-1), B = 551 cm(-1); C = 3500 cm(-1)). For 5 10Dq and B were determined (20580 cm(-1); 516 cm(-1), respectively) and compared with those for similar expanded cavity complexes [Co(Me(8)tricosatrieneN(6))](3+) and [Co(Me(5)tricosatrieneN(6))](3+).
机译:报告了六齿配体2,2,9,9-四(亚甲基胺)-4,7-二硫杂癸烷(EtN(4)S(2)amp)的合成。配体是其中链的分支发生在除供体原子以外的原子上的类型。分离并表征了钴(II​​I)配合物[Co(EtN(4)S(2)amp)](3+)(1)。合成方法还产生了许多副产物,特别是2,9,9-三(亚甲基胺)-9-亚甲基羟基-4,7-二硫杂癸烷(Et(HO)N(3)S(2)amp)和十一元侧链大环配体6,10-二甲基-6,10-双(亚甲基胺)-1,4-二硫-8-氮杂环十一碳烯-(dmatue)。配合物[Co(Et(HO)N(3)S(2)amp)](3+)(2),其中醇与金属离子配位,和[Co(dmatue)Cl](2+ )(4)进行了分离和表征。 Et(HO)N(3)S(2)amp还与钴(III)络合生成两种异构体-[Co(Et(HO)N(3)S(2)amp)Cl](2+) (endo-3)和exo- [Co(Et(HO)N(3)S(2)amp)Cl](2+)(exo-3),均带有未配位的醇基。内含3的醇顺式定位,而exo-3反式定位于第六个金属配位点。 1与异丁醛,低聚甲醛和碱在二甲基甲酰胺中的反应生成包封的复合物[Co(1,5,5,9,13,13-六甲基-18,21-二硫代-3,7,11,15-四氮杂双环[7.7 .6] docosa- 3,14-diene)](ClO4)(3)。 2H(2)O([Co(Me(6)docosadieneN(4)S(2))](3+)(5)。所有配合物均已通过单晶X射线研究表征。低温(11已在具有自旋允许(1)A(1g)-> T-1(1g)和(1)A(1g)-> T-1(2g)的Nafion薄膜中测量了1的K)吸收光谱。禁止自旋(1)A(1g)-> T-3(1g)和(1)A(1g)-> T-3(2g)谱带。确定八面体配体场参数(10Dq = 22570 cm(-1),B = 551 cm(-1); C = 3500 cm(-1))。对于5个10Dq和B,分别确定为20580 cm(-1); 516 cm(-1)和相比那些类似的扩大腔络合物[Co(Me(8)triosatrieneN(6))](3+)和[Co(Me(5)triosatrieneN(6))](3+)。

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