Synthetic And Spectroscopic Studies of Metal Carboxylate Dimers
Synthetic And Spectroscopic Studies of Metal Carboxylate Dimers
Telser, Joshua A.
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for Rh 2 C 12 H 18 N 2 8 : C, 27.50; H, 3.46; N, 5.34. Found: C, 27.54; H, 3.53; N, 5.02. Bi s ( tri phenyl phosphi ne ) tetraki s ( tri f 1 uoroacetato )di rhodi um( 1 1 ) This complex was synthesized following the procedure of Cotton and co-workers. 111 Rh 2 (0 3 CCF 3 ) 4 (0.050 g, 0.076 mmol) was dissolved in methanol (5 mL). Triphenylphosphine (0.040 g, 0.15 mmol) was dissolved in hot methanol (~5 mL). This solution was added to the blue Rh 2 (0 2 CCF 3 ) 4 (CH 3 0H) 2 solution to give an ...immediate dark brown color. 119 The solution quickly became colorless and purplish brown needle crystals were deposited. Filtration and washing with methanol afforded 0.085 g (0.075 mmol, 942). Anal. Calcd. for Rh 2 C 44 H 30 P 2 F 12 8 : C, 44.66; H, 2.56; P, 5.23. Found: C, 44.18; H, 2.67; P, 5.18. Orange Rh 2 (but) 4 (PPh 3 ) 2 was synthesized in the same manner in 822 yield. Anal. Calcd. for Rh 2 C 52 H 58 P 2 8 : C, 57.89; H, 5.43; P, 5.74. Found: C, 58.07; H, 5.40; P, 5.88. Bis (tri phenyl phosphite)tetrakis(trifluoroacetato)dirhodium(II) Rh 2 (0 2 CCF 3 ) 4 (0.178 g, 0.286 mmol) was dissolved in methanol (10 mL).
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