Balzani Vincenzo, Bandmann Heinz, Ceroni Paola, Giansante Carlo, Hahn Uwe, Klärner Frank-Gerrit, Müller Ute, Müller Walter M, Verhaelen Carla, Vicinelli Veronica, Vögtle Fritz
Dipartimento di Chimica G. Ciamician, Università di Bologna, Italy.
J Am Chem Soc. 2006 Jan 18;128(2):637-48. doi: 10.1021/ja056615j.
We have investigated the spectroscopic and electrochemical behavior of symmetric and unsymmetric first-, second-, and third-generation dendrimers comprising an electron-acceptor 4,4'-bipyridinium core (viologen type) and electron-donor 1,3-dimethyleneoxybenzene (Fréchet-type) dendrons. The quite strong fluorescence of the symmetrically and unsymmetrically disubstituted 1,3-dimethyleneoxybenzene units of the dendrons is completely quenched as a result of donor-acceptor interactions that are also evidenced by a low-energy tail in the absorption spectrum. In dichloromethane solution, the 4,4'-bipyridinium cores of the investigated dendrimers are hosted by a molecular tweezer comprising a naphthalene and four benzene components bridged by four methylene units. Host-guest formation causes the quenching of the tweezer fluorescence. The association constants, as measured from fluorescence and (1)H NMR titration plots, (i) are of the order of 10(4) M(-1), (ii) decrease on increasing dendrimer generation, and (iii) are slightly larger for the unsymmetric than for the symmetric dendrimer of the same generation. The analysis of the complexation-induced shifts of the temperature-dependent (1)H NMR signals of the host and guest protons confirms that the bipyridinium core is positioned inside the tweezer cavity and allows the conclusions that (i) shuttling of the tweezer from one to the other pyridinium ring is fast (DeltaG < 10 kcal/mol), (ii) in the case of the unsymmetric dendrimers, the less substituted pyridinium ring is preferentially complexed in apolar solvents, and (iii) complexation of the 4,4'-bipyridinium core proceeds by clipping for the symmetric dendrimers and by threading in the case of unsymmetric ones. Host-guest formation causes a displacement of the first reduction wave of the 4,4'-bipyridinium unit toward more negative potential values, whereas the second reduction wave is unaffected. These results show that the host-guest complexes between the tweezer and the dendrimers are stabilized by electron donor-acceptor interactions and can be reversibly assembled/disassembled by electrochemical stimulation.
我们研究了包含电子受体4,4'-联吡啶鎓核心(紫精型)和电子供体1,3-二亚甲基氧基苯(弗雷谢型)树枝状分子的对称和不对称第一代、第二代和第三代树枝状分子的光谱和电化学行为。树枝状分子中对称和不对称二取代的1,3-二亚甲基氧基苯单元的相当强的荧光由于供体-受体相互作用而完全猝灭,吸收光谱中的低能量尾部也证明了这种相互作用。在二氯甲烷溶液中,所研究树枝状分子的4,4'-联吡啶鎓核心由一个分子镊子容纳,该分子镊子由一个萘和四个由四个亚甲基单元桥连的苯组分组成。主客体形成导致镊子荧光猝灭。从荧光和(1)H NMR滴定曲线测得的缔合常数:(i) 约为10(4) M(-1),(ii) 随树枝状分子代数增加而降低,(iii) 同一代的不对称树枝状分子的缔合常数略大于对称树枝状分子。对主体和客体质子的温度依赖性(1)H NMR信号的络合诱导位移的分析证实,联吡啶鎓核心位于镊子腔内,并得出以下结论:(i) 镊子在一个吡啶鎓环和另一个吡啶鎓环之间的穿梭很快(ΔG < 10 kcal/mol),(ii) 在不对称树枝状分子的情况下,取代较少的吡啶鎓环在非极性溶剂中优先络合,(iii) 对称树枝状分子的4,4'-联吡啶鎓核心的络合通过夹断进行,不对称树枝状分子则通过穿线进行。主客体形成导致4,4'-联吡啶鎓单元的第一个还原波向更负的电位值位移,而第二个还原波不受影响。这些结果表明,镊子与树枝状分子之间的主客体络合物通过电子供体-受体相互作用得以稳定,并且可以通过电化学刺激进行可逆组装/拆卸。