The dialkyl malonate derived 1,3‐diphosphines R2C(CH2PPh2)2(R=
- NSF-PAR ID:
- 10249053
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Chemistry – A European Journal
- Volume:
- 27
- Issue:
- 39
- ISSN:
- 0947-6539
- Page Range / eLocation ID:
- p. 10021-10039
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Reactions of {(C 6 F 5 )Pt[S(CH 2 CH 2 -) 2 ](μ-Cl)} 2 and R 3 P yield the bis(phosphine) species trans -(C 6 F 5 )(R 3 P) 2 PtCl [R = Et ( Pt'Cl ), Ph, ( p -CF 3 C 6 H 4 ) 3 P; 88-81 %]. Additions of Pt'Cl and H(C≡C) n H ( n = 1, 2; HNEt 2 , 20 mol % CuI) give Pt'C 2 H (37 %, plus Pt'I , 16 %) and Pt'C 4 H (88 %). Homocoupling of Pt'C 4 H under Hay conditions (O 2 , CuCl, TMEDA, acetone) gives Pt'C 8 Pt' (85 %), but Pt'C 2 H affords only traces of Pt'C 4 Pt' . However, condensation of Pt'C 4 H and Pt'Cl (HNEt 2 , 20 mol % CuI) yields Pt'C 4 Pt' (97 %). Hay heterocouplings of Pt'C 4 H or trans -( p -tol)(Ph 3 P) 2 Pt(C≡C) 2 H ( Pt*C 4 H ) and excess HC≡CSiEt 3 give Pt'C 6 SiEt 3 (76 %) or Pt*C 6 SiEt 3 (89 %). The latter and wet n -Bu 4 N + F - react to yield labile Pt*C 6 H (60 %). Hay homocouplings of Pt*C 4 H and Pt*C 6 H give Pt*C 8 Pt* (64 %) and Pt*C 12 Pt* (64 %). Reaction of trans -(C 6 F 5 )( p -tol 3 P) 2 PtCl ( PtCl ) and HC≡CH (HNEt 2 , 20 mol % CuI) yields only traces of PtC 2 H . However, an analogous reaction with HC≡CSiMe 3 gives PtC 2 SiMe 3 (75 %), which upon treatment with silica yields PtC 2 H (77 %). An analogous coupling of trans -(C 6 F 5 )(Ph 3 P) 2 PtCl with H(C≡C) 2 H gives trans -(C 6 F 5 )(Ph 3 P) 2 Pt(C≡C) 2 H (34 %). Advantages and disadvantages of the various trans -(Ar)(R 3 P) 2 Pt end-groups are analyzed.more » « less
-
Reaction of ( p -tol 3 P) 2 PtCl 2 and Me 3 Sn(CC) 2 SiMe 3 (1 : 1/THF/reflux) gives monosubstituted trans -Cl( p -tol 3 P) 2 Pt(CC) 2 SiMe 3 (63%), which with wet n -Bu 4 N + F − yields trans -Cl( p -tol 3 P) 2 Pt(CC) 2 H ( 2 , 96%). Hay oxidative homocoupling (O 2 /CuCl/TMEDA) gives all- trans -Cl( p -tol 3 P) 2 Pt(CC) 4 Pt(P p -tol 3 ) 2 Cl ( 3 , 68%). Reaction of 3 and Me 3 Sn(CC) 2 SiMe 3 (1 : 1/rt) affords monosubstituted all- trans -Cl( p -tol 3 P) 2 Pt(CC) 4 Pt(P p -tol 3 ) 2 (CC) 2 SiMe 3 (46%), which is converted by a similar desilylation/homocoupling sequence to all- trans -Cl[( p -tol 3 P) 2 Pt(CC) 4 ] 3 Pt(P p -tol 3 ) 2 Cl ( 7 ; 79%). Reaction of ( p -tol 3 P) 2 PtCl 2 and excess H(CC) 2 SiMe 3 (HNEt 2 /cat. CuI) gives trans -Me 3 Si(CC) 2 Pt(P p -tol 3 ) 2 (CC) 2 SiMe 3 (78%), which with wet n -Bu 4 N + F − affords trans -H(CC) 2 Pt(P p -tol 3 ) 2 (CC) 2 H (96%). Hay oxidative cross coupling with 2 (1 : 4) gives all- trans -Cl[( p -tol 3 P) 2 Pt(CC) 4 ] 2 Pt(P p -tol 3 ) 2 Cl ( 10 , 36%) along with homocoupling product 3 (33%). Reaction of 3 and Me 3 Sn(CC) 2 SiMe 3 (1 : 2/rt) yields all- trans -Me 3 Si(CC) 2 ( p -tol 3 P) 2 Pt(CC) 4 Pt(P p -tol 3 ) 2 (CC) 2 SiMe 3 ( 17 , 77%), which with wet n -Bu 4 N + F − gives all- trans -H(CC) 2 ( p -tol 3 P) 2 Pt(CC) 4 Pt(P p -tol 3 ) 2 (CC) 2 H (96%). Reaction of 3 and excess Me 3 P gives all- trans -Cl(Me 3 P) 2 Pt(CC) 4 Pt(PMe 3 ) 2 Cl ( 4 , 86%). A model reaction of trans -( p -tol)( p -tol 3 P) 2 PtCl and KSAc yields trans -( p -tol)( p -tol 3 P) 2 PtSAc ( 12 , 75%). Similar reactions of 3 , 7 , 10 , and 4 give all- trans -AcS[(R 3 P) 2 Pt(CC) 4 ] n Pt(PR 3 ) 2 SAc (76–91%). The crystal structures of 3 , 17 , and 12 are determined. The first exhibits a chlorine–chlorine distance of 17.42 Å; those in 10 and 7 are estimated as 30.3 Å and 43.1 Å.more » « less
-
CuI catalyzes reactions of cis -(R 2 C(CH 2 PPh 2 ) 2 )Pt(CCCCH) 2 and cis -(R 2 C(CH 2 PPh 2 ) 2 )PtI 2 in secondary amine solvents HNR’ 2 to give the title adducts [(R 2 C(CH 2 PPh 2 ) 2 )Pt(CCCC)] 4 ·(H 2 NR’ 2 + I − ) n (R/R’/ n = Me/Et/1, Me/((CH 2 CH 2 ) 2 O) 0.5 /3, Et/Et/1, Et/CH 2 CHCH 2 /1; 92–42%). Crystal structures of these or closely related species establish folded Pt 4 cores containing ammonium cation guests, with NH/ and NCH/CC hydrogen bonding. DOSY NMR experiments show that the host/guest relationship can be maintained in solution.more » « less
-
Abstract Herein we combine the subcomponent self‐assembly and integrative self‐sorting techniques with the well‐established platinum(II)‐pyridine coordination‐driven self‐assembly to report the quantitative synthesis and spectroscopic characterization of a heterometallic CuI‐PtIIquadrilateral
QL that is formed from a total of twelve molecular components from four unique species, including 5‐(pyridin‐4‐ylethynyl)picolinaldehyde (1 ),p ‐toluidine (2 ), [Cu(CH3CN4](PF6) (3 ), andcis ‐Pt(PEt3)2(OTf)2(4 ), in a 4:4:2:2 ratio. Despite the many different entities potentially forming from these four precursor units, the clean formation ofQL is mainly guided by the different coordination preferences of the metal ions3 and4 , and the design criteria inherent in compounds1 and2 . -
Abstract A new series of mono‐ and bis‐alkynyl CoIII(TIM) complexes (TIM=2,3,9,10‐tetramethyl‐1,4,8,11‐tetraazacyclotetradeca‐1,3,8,10‐tetraene) is reported herein. The
trans ‐[Co(TIM)(C2R)Cl]+complexes were prepared from the reaction betweentrans ‐[Co(TIM)Cl2]PF6and HC2R (R=tri(isopropyl)silyl or TIPS (1 ), ‐C6H4‐4‐tBu (2 ), ‐C6H4‐4‐NO2(3 a ), andN ‐mesityl‐1,8‐naphthalimide or NAPMes(4 a )) in the presence of Et3N. The intermediate complexes of the typetrans ‐[Co(TIM)(C2R)(NCMe)](PF6)(OTf),3 b and4 b , were obtained by treating3 a and4 a , respectively, with AgOTf in CH3CN. Furthermore, bis‐alkynyltrans ‐[Co(TIM)(C2R)2]PF6complexes,3 c and4 c , were generated following a second dehydrohalogenation reaction between3 b and4 b , respectively, and the appropriate HC2R in the presence of Et3N. These new complexes have been characterized using X‐ray diffraction (2 ,3 a ,4 a , and4 c ), IR,1H NMR, UV/Vis spectroscopy, fluorescent spectroscopy (4 c ), and cyclic voltammetry.