Tuning stoichiometry and supramolecular assembly in perfluorinated indazolato coinage metal complexes.
نویسندگان
چکیده
The reaction of 3-pentafluoroethyl-4,5,6,7-tetrafluoro-1-H-indazole [3-(C2F5)IndF4]H with Ag2O or [Cu(CH3CN)4]BF4 leads to the formation of two different types of complexes: a trinuclear {[3-(C2F5)IndF4]Ag}3 complex (1) in the case of silver, and an unprecedented type of pentanuclear complex [Et3NH]{Cu5[3-(C2F5)IndF4]6} (2) in the case of copper. When crystallised from Et2O, appears as a dimer with d(10)-d(10) interactions. When crystallized from toluene, affords the [(toluene)(1)(toluene)] adduct, testifying to its strong π-acid properties. The formation and the aggregation pattern of 1 and 2 can be traced to the extended aromaticity and high electron withdrawing properties of the perfluorinated [3-(C2F5)IndF4](-) indazolate.
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ورودعنوان ژورنال:
- Dalton transactions
دوره 42 28 شماره
صفحات -
تاریخ انتشار 2013