Department of Chemistry, Indian Institute of Technology, Bombay, Powai, Mumbai 400 076, India.
Inorg Chem. 2010 Nov 15;49(22):10606-16. doi: 10.1021/ic1016092. Epub 2010 Oct 14.
We have synthesized four examples of a cyclotriphosphazene ring appended with six boron-dipyrromethene dyes N(3)P(3)(BODIPY)(6) by adopting two different methods. In method I, 1 equiv of N(3)P(3)Cl(6) was treated with 6 equiv of meso-(o- or m- or p-hydroxyphenyl)boron-dipyrromethene in tetrahydrofuran (THF) in the presence of cesium carbonate. This afforded N(3)P(3)(BODIPY)(6) in yields ranging from 80 to 90%. In method II, we first prepared hexakis(p-formylphenoxy)cyclotriphosphazene N(3)P(3)(CHO)(6) by treating 1 equiv of N(3)P(3)Cl(6) with 6 equiv of 4-hydroxybenzaldehyde in the presence of cesium carbonate in THF. In the second step, N(3)P(3)(CHO)(6) was condensed with excess of pyrrole in the presence of catalytic amount of trifluoroacetic acid (TFA) in CH(2)Cl(2) at room temperature and afforded hexakis(p-phenoxy dipyrromethane)cyclotriphosphazene. In the last step, the hexakis(p-phenoxy dipyrromethane)cyclotriphosphazene was first oxidized with 6 equiv of DDQ in CH(2)Cl(2) at room temperature for 1 h followed by neutralization with triethylamine and further reaction with excess BF(3)·Et(2)O afforded the target N(3)P(3)(BODIPY)(6) in 16% yield. The route II was used only for the synthesis of one target compound whereas the route I was used for the synthesis of all four target compounds. The four compounds were characterized by mass, NMR, absorption, electrochemical, and fluorescence techniques. The crystal structure solved for one of the compounds revealed that the P(3)N(3) ring is slightly puckered and the six substituents were not interacting with each other and attained pseudo-axial and pseudo-equatorial positions. The photophysical studies in five different solvents indicated that the compounds exhibit large Stokes' shifts unlike reference monomeric BODIPYs indicating that the compounds are promising for fluorescence bioassays. The quantum yields and lifetimes of compounds 1-4 depends on the type of BODIPY unit attached to the cyclotriphosphazene ring.
我们通过两种不同的方法合成了四个环三磷腈环连接六个硼二吡咯甲烷染料 N(3)P(3)(BODIPY)(6)的例子。在方法 I 中,1 当量的 N(3)P(3)Cl(6)与 6 当量的间-(邻-或间-或对-羟基苯基)硼二吡咯甲烷在四氢呋喃(THF)中在碳酸铯存在下反应。这在 80 到 90%的产率范围内得到 N(3)P(3)(BODIPY)(6)。在方法 II 中,我们首先通过 1 当量的 N(3)P(3)Cl(6)与 6 当量的 4-羟基苯甲醛在 THF 中在碳酸铯存在下制备六(对甲酰基苯氧基)环三磷腈 N(3)P(3)(CHO)(6)。在第二步中,N(3)P(3)(CHO)(6)在催化量的三氟乙酸(TFA)存在下在室温下与过量的吡咯在 CH(2)Cl(2)中缩合,得到六(对苯氧基二吡咯甲烷)环三磷腈。在最后一步,首先用 6 当量的 DDQ 在室温下在 CH(2)Cl(2)中氧化六(对苯氧基二吡咯甲烷)环三磷腈 1 小时,然后用三乙胺中和,进一步用过量的 BF(3)·Et(2)O 反应,得到目标化合物 N(3)P(3)(BODIPY)(6),产率为 16%。路线 II 仅用于合成一种目标化合物,而路线 I 用于合成所有四种目标化合物。这四种化合物通过质谱、NMR、吸收、电化学和荧光技术进行了表征。一种化合物的晶体结构表明,P(3)N(3)环略有扭曲,六个取代基没有相互作用,达到了伪轴向和伪赤道位置。在五种不同溶剂中的光物理研究表明,与参考单体 BODIPY 相比,化合物表现出较大的斯托克斯位移,这表明化合物在荧光生物测定中很有前途。化合物 1-4 的量子产率和寿命取决于连接到环三磷腈环的 BODIPY 单元的类型。