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Tab. 2.8 Selected bond lengths and bond angles for 14c .
14 c · 2CH 3 CN
Bond lengths [Å]
Bond angles [ ]
Pd-P1
2.256(2)
P1-Pd-P2
86.98(7)
Pd-P1
2.252(2)
Cl1-Pd-Cl2
94.32(7)
Pd-Cl1
2.357(2)
Pd-Cl2
2.348(2)
C21-P1-C30
106.8(3)
C21-P1-C1
107.2(3)
P1-C21
1.817(7)
C30-P1-C1
106.4(3)
P1-C30
1.826(7)
P1-C1
1.839(7)
C3-P2-C2
108.2(3)
C3-P2-C12
106.8(3)
P2-C3
1.822(7)
C2-P2-C12
106.6(3)
P2-C2
1.833(7)
P2-C12
1.833(7)
Tab. 2.9 Selected bond lengths and bond angles for 14d .
14d · CH 3 CN
Bond lengths [Å]
Bond angles [ ]
Pd-P1
2.2780(10)
P1-Pd-P2
88.85(4)
Pd-P1
2.3041(11)
Cl1-Pd-Cl2
91.55(4)
Pd-Cl1
2.3462(11)
Pd-Cl2
2.3513(11)
C1-P1-C11
100.34(16)
C1-P1-C26
112.15(15)
P1-C26
1.862(3)
C11-P1-C26
104.56(14)
P1-C11
1.852(3)
P1-C1
1.843(3)
C2-P2-C41
111.54(16)
C2-P2-C56
96.03(15)
P2-C56
1.872(3)
C41-P2-C56
105.02(15)
P2-C41
1.856(4)
P2-C2
1.848(3)
atoms tends towards a tetrahedral environment. The Pd-Cl bond lengths are sur-
prisingly constant. They vary between 2.3462(11) Å for 14d and 2.357(2) Å and
consists of slightly longer values for 14b , c . As a first conclusion one can say that
the amount of substitutions of the phenyl rings is significantly correlated to the
increasing Pd-P bond lengths, widening of the P1-Pd-P2 bond angle and to high
distortion from the square-planar coordination geometry [56]. Furthermore, the
crystal structures of 14 c , d indicate that in both complexes isopropyl substituents
are located in axial positions above and below the coordination plane. This charac-
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