Synthesis of selectively 4-substituted 9,9'-spirobifluorenes and modulation of their photophysical properties
Abstrakt
Synthesis of selectively 4-substituted 9,9'-spirobifluorenes was accomplished by using catalytic [2 + 2 + 2]-cyclotrimerization of specifically substituted diynols with alkynes to the corresponding fluorenols. Further synthetic transformations provided the target molecules.
The measurement of the photophysical properties of the prepared 4-substituted 9,9'-spirobifluorenes revealed that their emission maxima depended on the electronic properties of the substituents present in the para position: the presence of an electron accepting group strongly favored the maxima red shift toward the blue VIS region (CF3 lambda(max) = 361 nm vs. MeO lambda(max) = 330 nm).
Adding further substituents (aryl or arylethynyl moieties) on the phenyl ring in position 4 did not lead to a dramatic improvement in the emission maxima (CF3C6H4, lambda(max) = 369 nm, CF3C6H4C C, lambda(max) = 370 nm), but increased their quantum yields considerably. In addition, a series of 9,9'-spirobifluorenes possessing various extended pi-systems (pyrene, anthracene, etc.) were synthesized.
In general, the emission maxima pattern reflected that of the parent pi-systems, but they were red shifted by 10-30 nm. Finally, also a 1-[4-(9,9'-spirobifluorene-4-yl)phenyl]-2-aryl-ortho-carborane was prepared.
These data thus may provide guidelines for further design of 9,9'-spirobifluorenes with tailored properties.