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首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Thioether-iodine charge-transfer complexes. Synthesis and low temperature single-crystal structures of complexes of penta-, hexa- and octa-dentate homoleptic thioether macrocycles
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Thioether-iodine charge-transfer complexes. Synthesis and low temperature single-crystal structures of complexes of penta-, hexa- and octa-dentate homoleptic thioether macrocycles

机译:硫醚-碘电荷转移复合物。五齿,六齿和八齿均硫硫醚大环配合物的合成和低温单晶结构

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Charge-transfer complexes 2([15]aneS(5),).7I(2), I ([15]aneS(5), = 1,4,7,10, 13-pentathiacyclopentadecane), [18]aneS(6).I-2 2, [18]aneS(6).4I(2)3 ([18]aneS(6) = 1,4,7,10,13,16-hexathiacyclooctadecane) [24]aneS(8).I(2)4 and [24]aneS(8).6I(2)5 ([24]aneS(8) = 1,4,7,10,13,16,19,22-octathiacyclotetracosane) have been prepared and their structures and solution properties investigated. The compounds were prepared by slow evaporation of solutions containing I-2 and the appropriate thioether macrocycle in CH2CI2. The single-crystal structure determination of I shows three I, molecules coordinated to three exo oriented S donors [S(I)-I(I) 2.797(3), I(1)-I(1') 2.798(2), S(4)-I(4) 2.885(4), 1(4)-I(4') 2.764(2), S(7)-I(7) 2.828(3) and 1(7)-I(7') 2.779(2) Angstrom; S(I)-I(I)-I(1') 178.39(8), S(4)-I(4)-I(4') 171.12(8), S(7)-I(7)-I(7') 178.80(8)degrees]. The fourth I,molecule (with a site occupancy of 0.5) lies close to S(IO) [I(IO)-S(10) 2.839(5) Angstrom], the bond distance 1(10)-I(10') 2.674(3) Angstrom being unusually short. Compound 2 is an example of a 1:1 I-2,:macrocycle adduct and shows symmetrically bridging I-2 molecules [S(I)-I(I) 3.099(2), I(1)-I(1') 2.7881(10) Angstrom; 8(1)-I(1)-I(1') 178.68(4)degrees; i I - x, 1 - y, 1 - z] between [18]aneS(6), macrocycles. Compound 3 is the first example of an adduct between I-2, and a homoleptic thioether macrocycle which shows both exo [S(I)-I(I) 2.838(2), I(1)-I(1') 2.7875(6) Angstrom; S(1)-I(1)-I(1') 174.95(4)degrees] and endo [S(4)-I(4) 2.792(2), I(4)-I(4') 2.8067(7) Angstrom S(4)-I(4)-I(4') 174.43(4)degrees] co-ordination of I-2, molecules. The endo-oriented I-2, molecules occupy space above and below the macrocyclic plane with the macrocycle adopting a sigmoid conformation. The single-crystal structure determination of the I : 1 adduct 4 shows symmetrically bridging I-2 molecules [8(1)-I(1) 3.215(2) and I(1)-I(1') 2.758(2) Angstrom; S(1)-I(1)-I(IL) 172.75(3)degrees; i -x, -y, -z] which are a characteristic of this stoichiometry. Compound 5 contains endo- and exo-oriented S donors within the same adduct [1(1)-I(1') 2.7861(8), 1(4)-I(4') 2.7937(8), 1(7)-I(7') 2.8345(8), S(I)-I(I) 2.821(2), S(4)-I(4) 2.815(2), S(7)-I(7) 2.741(2) Angstrom; S(I)-I(I)-I(1') 170. i 5(5), 8(4)-I(4)-I(4') 177.41(5), S(7)-I(7)-I(7') 177.24(5)degrees]. These results are discussed in the context of the stability and characteristics of thioether crown-iodine charge-transfer complexes, and a qualitative MO diagram is proposed to account for the shorter I-I distances in bridging I-2 fragments compared to those in terminally bound I-2. [References: 49]
机译:电荷转移络合物2([15] aneS(5),)。7I(2),I([15] aneS(5),= 1,4,7,10,13-pentathiacyclopentadecane),[18] aneS( 6).I-2 2,[18] aneS(6).4I(2)3([18] aneS(6)= 1,4,7,10,13,16-六硫代环十八烷)[24] aneS(8 ).I(2)4和[24] aneS(8).6I(2)5([24] aneS(8)= 1,4,7,10,13,16,19,22-octathiacyclotetracosane)已经制备并研究其结构和溶液性质。通过缓慢蒸发包含I 2和合适的硫醚大环化合物的CH 2 Cl 2溶液来制备化合物。 I的单晶结构确定显示三个I分子与三个外向取向的S供体[S(I)-I(I)2.797(3),I(1)-I(1')2.798(2), S(4)-I(4)2.885(4),1(4)-I(4')2.764(2),S(7)-I(7)2.828(3)和1(7)-I( 7')2.779(2)埃; S(I)-I(I)-I(1')178.39(8),S(4)-I(4)-I(4')171.12(8),S(7)-I(7)- I(7')178.80(8)degrees]。第四个I分子(位点占用为0.5)位于S(IO)[I(IO)-S(10)2.839(5)埃)附近,键距为1(10)-I(10') 2.674(3)埃异常短。化合物2是1:1 I-2 ::大环加合物的一个例子,它显示对称桥接的I-2分子[S(I)-I(I)3.099(2),I(1)-I(1') 2.7881(10)埃; 8(1)-I(1)-I(1')178.68(4)度; [18] aneS(6)之间的i-x,1- y,1- z]宏周期。化合物3是I-2与均相硫醚大环之间加合物的第一个例子,该化合物同时显示exo [S(I)-I(I)2.838(2),I(1)-I(1')2.7875( 6)埃; S(1)-I(1)-I(1')174.95(4)度]和内点[S(4)-I(4)2.792(2),I(4)-I(4')2.8067( 7)I-2分子的Angstrom S(4)-I(4)-I(4')174.43(4)度配位。内向的I-2分子在大环平面的上方和下方占据空间,大环采用S形构象。 I 1:1加合物4的单晶结构确定显示对称桥接的I-2分子[8(1)-I(1)3.215(2)和I(1)-I(1')2.758(2)埃; S(1)-I(1)-I(IL)172.75(3)度; i -x,-y,-z]是该化学计量的特征。化合物5在同一加合物中包含内向和外向S供体[1(1)-I(1')2.7861(8),1(4)-I(4')2.7937(8),1(7) -I(7')2.8345(8),S(I)-I(I)2.821(2),S(4)-I(4)2.815(2),S(7)-I(7)2.741( 2)埃; S(I)-I(I)-I(1')170。i 5(5),8(4)-I(4)-I(4')177.41(5),S(7)-I( 7)-I(7')177.24(5)度]。在硫醚冠碘电荷转移复合物的稳定性和特性的背景下讨论了这些结果,并提出了定性的MO图,以说明桥接I-2片段时的II距离要比末端结合的I-中的距离短。 2。 [参考:49]

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