Chelating Phosphorus-An O, C, O-Coordinating Pincer-Type Ligand Coordinating P^III and P^V Centres

The sequence of reactions of the phosphorus-containing aryllithium compound 5-t-Bu-1,3-[(P(O)(O-i-Pr)₂ ]₂ C₆ H₂ Li (ArLi) with Ph₂ PCl, KMnO₄ , elemental sulfur and elemental selenium, respectively, gave the aryldiphenylphosphane chalcogenides 5-t-Bu-1,3-[(P(O)(O-i-Pr)₂ ]₂ C₆ H₂ P(E)Ph₂ (1, E=O; 2, E=S; 3, E=Se). Compound 1 partially hydrolysed giving [5-t-Bu-1-{(P(O)(O-i-Pr)₂ }-3-{(P(O)(OH)₂ }C₆ H₂ ]P(O)Ph₂ (4). The reaction of ArLi with PhPCl₂ provided the benzoxaphosphaphosphole [1(P), 3(P)-P(O)(O-i-Pr)OPPh-6-t-Bu-4-P(O)(O-i-Pr)₂ ]C₆ H₂ P (5i) as a mixture of the two diastereomers. The oxidation of 5i with elemental sulfur gave the benzoxaphosphaphosphole sulfide [1(P), 3(P)-P(O)(O-i-Pr)OP(S)Ph-6-t-Bu-4-P(O)(O-i-Pr)₂ ]C₆ H₂ (5) as pair of enantiomers P1(R), P3(S)/P1(S), P3(R) of the diastereomer (RS/SR)-5 (5b). The aryldiphenylphosphane 5-t-Bu-1,3-[(P(O)(O-i-Pr)₂ ]₂ C₆ H₂ PPh₂ (6) was obtained from the reaction of the corresponding aryldiphenylphosphane sulfide 2 with either sodium hydride, NaH, or disodium iron tetracarbonyl, Na₂ Fe(CO)₄ . The oxidation of the aryldiphenylphosphane 6 with elemental iodine and subsequent hydrolysis yielded the aryldiphenyldioxaphosphorane 9-t-Bu-2,6-(OH)-4,4-Ph₂ -3,5-O₂ -2,6-P₂ -4λ⁵ -P-[5.3.1.0]-undeca-1(10),7(11),8-triene (7). Both of its diastereomers, (RR/SS)-7 (7a) and (RS/SR)-7 (7b), were separated as their chloroform and i-propanol solvates, 7a⋅2CHCl₃ and 7b⋅i-PrOH, respectively. DFT calculations accompanied the experimental work.