Abstract
Although the triple-decker complex [Cp*Fe(µ,η&sup5;:η&sup5;-P₅)Mo(CO)&sub3;] (2) was first reported 26 years ago, its reactivity has not yet been explored. Herein, we report a new high-yielding synthesis of 2 and the isolation of its new polymorph (2'). In addition, we study its reactivity towards AgI and CuI ions. The reaction of 2 with Ag[BF&sub4;] selectively produces the coordination compound [Ag{Cp*Fe(µ,η&sup5;:η&sup5;-P₅)Mo(CO)&sub3;}&sub2;][BF&sub4;] (3). Its reaction with Ag[TEF] and Cu[TEF] ([TEF]- = [Al{OC(CF&sub3;)&sub3;}&sub4;]-) leads to the selective formation of the complexes [Ag{Cp*Fe(µ,η&sup5;:η&sup5;-P₅)Mo(CO)&sub3;}&sub2;][TEF] (4) and [Cu{Cp*Fe(µ,η&sup5;:η&sup5;-P₅)Mo(CO)&sub3;}&sub2;][TEF] (5), respectively. The X-ray structures of compounds 3⁻5 each show an MI ion (MI = AgI, CuI) bridged by two P atoms from two triple-decker complexes (2). Additionally, four short MI···CO distances (two to each triple-decker complex 2) participate in stabilizing the coordination sphere of the MI ion. Evidently, the X-ray structure for compound 3 shows a weak interaction of the AgI ion with one fluorine atom of the counterion [BF&sub4;]-. Such an Ag···F interaction does not exist for compound 4. These findings demonstrate the possibility of using triple-decker complex 2 as a ligand in coordination chemistry and opening a new perspective in the field of supramolecular chemistry of transition metal compounds with phosphorus-rich complexes.