Home Physical Sciences Crystal structure of trans-dichlorido-(1,3-dimesityl-1H-imidazol-2(3H)-ylidene)-(5-methyl-3,4-dihydro-2H-pyrrole-κN)palladium(II), C25H31Cl2N3OPd
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Crystal structure of trans-dichlorido-(1,3-dimesityl-1H-imidazol-2(3H)-ylidene)-(5-methyl-3,4-dihydro-2H-pyrrole-κN)palladium(II), C25H31Cl2N3OPd

  • Kai-Xin Sun , Xiang-Ting Wu and Guo-Xing Li EMAIL logo
Published/Copyright: February 1, 2019

Abstract

C25H31Cl2N3OPd, orthorhombic, Pbca (no. 61), a = 9.4083(4) Å, b = 17.1334(8) Å, c = 31.9251(14) Å, V = 5146.2(4) Å3, Z = 8, Rgt(F) = 0.0600, wRref(F2) = 0.1232, T = 293(2) K.

CCDC no.: 1889570

The crystal structure is shown in the figure. Tables 1 and 2 contain details on crystal structure and measurement conditions and a list of the atoms including atomic coordinates and displacement parameters.

Table 1:

Data collection and handling.

Crystal:Yellow prisma
Size:0.18 × 0.13 × 0.10 mm
Wavelength:Mo Kα radiation (0.71073 Å)
μ:0.95 mm−1
Diffractometer, scan mode:Bruker APEX-II CCD, φ and ω
θmax, completeness:25.0°, 97%
N(hkl)measured, N(hkl)unique, Rint:39904, 4516, 0.050
Criterion for Iobs, N(hkl)gt:Iobs > 2 σ(Iobs), 3679
N(param)refined:297
Programs:Bruker [1], SHELX [2]
Table 2:

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2).

AtomxyzUiso*/Ueq
Pd10.79736(4)0.49971(2)0.64596(2)0.03921(17)
Cl10.94877(17)0.57707(10)0.60706(5)0.0639(4)
Cl20.65567(15)0.42889(8)0.69055(5)0.0523(4)
N10.5803(5)0.5282(3)0.58179(15)0.0536(13)
N20.5327(5)0.5986(2)0.63581(15)0.0469(12)
N30.9718(5)0.4373(3)0.66681(14)0.0479(11)
O11.1510(5)0.3526(3)0.66404(14)0.0750(13)
C10.6275(5)0.5471(3)0.62058(17)0.0394(12)
C20.4576(8)0.5688(4)0.5729(2)0.083(2)
H20.40600.56660.54810.099*
C30.4264(7)0.6120(4)0.6065(2)0.077(2)
H30.34830.64480.60960.093*
C40.5381(6)0.6341(3)0.67653(19)0.0469(14)
C50.4510(6)0.6057(3)0.7083(2)0.0538(15)
C60.4666(6)0.6378(3)0.7478(2)0.0580(16)
H60.40990.61920.76940.070*
C70.5636(6)0.6966(3)0.75627(19)0.0538(15)
C80.6436(6)0.7256(3)0.72302(19)0.0526(15)
H80.70710.76620.72810.063*
C90.6321(6)0.6962(3)0.68249(18)0.0461(13)
C100.3398(7)0.5435(4)0.7006(2)0.074(2)
H10A0.29910.52760.72680.111*
H10B0.38320.49930.68730.111*
H10C0.26650.56400.68280.111*
C110.5822(8)0.7287(4)0.7998(2)0.080(2)
H11A0.52600.69880.81910.120*
H11B0.55190.78220.80040.120*
H11C0.68050.72560.80760.120*
C120.7161(7)0.7304(4)0.64717(19)0.0636(18)
H12A0.75680.77910.65590.095*
H12B0.65470.73900.62360.095*
H12C0.79060.69500.63940.095*
C130.6476(6)0.4714(3)0.55509(18)0.0487(14)
C140.7399(7)0.4959(4)0.52394(19)0.0571(16)
C150.8086(7)0.4405(4)0.50041(19)0.0565(16)
H150.87140.45620.47950.068*
C160.7861(7)0.3611(4)0.5072(2)0.0566(16)
C170.6884(7)0.3396(4)0.5367(2)0.0593(17)
H170.66980.28680.54040.071*
C180.6150(6)0.3934(3)0.56165(18)0.0533(15)
C190.5070(7)0.3668(4)0.5928(2)0.0698(19)
H19A0.53170.38620.62010.105*
H19B0.50480.31080.59340.105*
H19C0.41510.38630.58500.105*
C200.7599(9)0.5821(4)0.5145(2)0.074(2)
H20A0.83200.58830.49350.110*
H20B0.78830.60880.53960.110*
H20C0.67200.60370.50450.110*
C210.8627(9)0.3012(4)0.4811(2)0.089(2)
H21A0.93040.27390.49820.134*
H21B0.91130.32680.45850.134*
H21C0.79520.26470.46990.134*
C221.0134(6)0.4276(4)0.71026(18)0.0556(15)
H22A0.93510.40750.72690.067*
H22B1.04510.47670.72220.067*
C231.1343(6)0.3691(4)0.70834(19)0.0559(15)
H23A1.22070.39120.71990.067*
H23B1.11060.32210.72370.067*
C241.0513(6)0.3933(4)0.64425(18)0.0557(16)
C251.0491(8)0.3828(5)0.59802(19)0.083(2)
H25A0.95600.39490.58750.124*
H25B1.07220.32970.59130.124*
H25C1.11760.41700.58540.124*

Source of material

The title complex was easily obtained by our very recent reported method [3]. Single crystals were grown in a mixture of ethyl acetate and petroleum ether.

Experimental details

Hydrogen atoms were introduced using the HFIX command in the SHELXL7 program [2]. Vinylic and aromatic C—H distances were restrained to 0.93 Å with Uiso values to be 1.2Ueq(C) [1], [4].

Comment

N-heterocyclic carbene (NHC)-palladium(II) complexes have been good catalyst for the Suzuki-Miyaura coupling of aryl chlorides with arylboronic acids under mild conditions [5], [6], [7], [8], [9]. However, to the best of our knowledge, no manuscript was reported on the NHC-Pd(II) complexes catalyzed selective mono-Suzuki-Miyaura coupling of dichlorobenzenes with arylboronic acids till our recent paper was published [3]. In our recent paper, the title product, showed efficient catalytic activity for the highly selective mono-Suzuki-Miyaura coupling of dichlorobenzenes with arylboronic acids. The crystal structure of the title compound is of interest to investigate the structure-activity relationship of such complexes.

The Pd center in the title compound shows slightly distorted square-planar geometry with four ligands. The bond lengthes around the Pd center ranges in the normal ones [10]. For example, the bond length of Pd(1)—C(1) is 1.967(5) Å; Pd(1)—N(3) is 2.069(4) Å; Pd(1)—Cl(1) is 2.3084(16) Å and Pd(1)—Cl(2) is 2.2970(15) Å. The bond angles around the Pd center are shown as the following: C(1)—Pd(1)—N(3) = 172.0(2)°; C(1)—Pd(1)—Cl(2) = 90.10(16)°; N(3)—Pd(1)—Cl(2) = 89.32(13)°; C(1)—Pd(1)—Cl(1) = 92.45(16)°; N(3)—Pd(1)—Cl(1) = 88.87(13)°; Cl(2)—Pd(1)—Cl(1) = 174.23(6)°.

Acknowledgements

We acknowledge the financial support from Wenzhou University for the publication fee.

References

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Received: 2018-10-30
Accepted: 2019-01-08
Published Online: 2019-02-01
Published in Print: 2019-03-26

©2019 Kai-Xin Sun et al., published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 Public License.

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  73. Crystal structure of methyl 4-acetoxybenzoate, C10H10O4
  74. Crystal structure of catena-poly[(bis(μ-1,1′-[(5-methoxy-2,4,6-trimethyl-1,3-phenylene)bis(methylene)]bis(1H-1,2,4-triazole)-κ2N:N′)-bis(isothiocyanato-κN)manganese(II)], C34H40MnN14O2S2
  75. Crystal structure of N-(2-methylphenyl)(propan-2-yloxy)carbothioamide, C11H15NOS
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