Hexa Boron-Dipyrromethene Cyclotriphosphazenes: Synthesis, Crystal Structure, and Photophysical Properties

We have synthesized four examples of a cyclotriphosphazene ring appended with six boron-dipyrromethene dyes N3P3(BODIPY)(6) by adopting two different methods. In method I, 1 equiv of N3P3Cl6 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 N3P3(BODIPY)(6) in yields ranging from 80 to 90%. In method II, we first prepared hexakis(p-formylphenoxy)cyclotriphosphazene N3P3(CHO)(6) by treating 1 equiv of N3P3Cl6 with 6 equiv of 4-hydroxybenzaldehyde in the presence of cesium carbonate in THF. In the second step, N3P3(CHO)(6) was condensed with excess of pyrrole in the presence of catalytic amount of trifluoroacetic acid (TFA) in CH2Cl2 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 CH2Cl2 at room temperature for 1 h followed by neutralization with triethylamine and further reaction with excess BF3 center dot Et2O afforded the target N3P3(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 P3N3 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.