兩個基于呋喃-3-酮配體的鈀(Ⅱ)化合物的合成、晶體結構和光譜性質

趙明霞　熊麗琴　蔡永樂　常　進　任紅玉　張華北　齊傳民＊,

(1山西工程技術學院采礦工程系，陽泉045000) (2上海交通大學生物醫學工程學院，上海200025)

(3北京師范大學化學學院，教育部放射性藥物重點實驗室，北京100875)

兩個基于呋喃-3-酮配體的鈀(Ⅱ)化合物的合成、晶體結構和光譜性質

趙明霞1熊麗琴2蔡永樂1常進3任紅玉3張華北3齊傳民＊,3

(1山西工程技術學院采礦工程系，陽泉045000) (2上海交通大學生物醫學工程學院，上海200025)

(3北京師范大學化學學院，教育部放射性藥物重點實驗室，北京100875)

合成了2個鈀(Ⅱ)化合物Pd(L1)2(1)和Pd(L2)2(2)，(L1=(Z)-4-((對甲苯胺基)亞甲基)-2，2，5，5-四甲基二氫呋喃-3(2H)-酮，L2=(Z) -4-((鄰甲苯胺基)亞甲基)-2，2，5，5-四甲基二氫呋喃-3(2H)-酮)，并利用元素分析，紅外光譜，核磁共振氫譜，紫外光譜和X射線單晶衍射等手段對其結構進行了表征。X射線單晶衍射表明，化合物1和2中包含多種弱相互作用。在化合物1中，呋喃環上氧原子和苯環上的甲基氫原子之間形成氫鍵，氫鍵橋聯分子形成了一條平行于c軸方向的一維鏈結構，一維鏈之間通過C-H…H-C和C-H…C弱相互作用形成了三維超分子結構。在化合物2中，分子之間通過C-H…H-C和C-H…C弱相互作用形成了一個二維層狀結構。

合成；Pd(Ⅱ)；呋喃-3-酮；晶體結構；弱相互作用

The understanding of various molecular interactions plays a major role in supramolecular chemistry and crystal engineering[1-6].The knowledge of structural motifs generated by such interactions can be utilized in the design of novel materials with desirable physical and chemical properties[7].Hydrogen bonding interactions and π-π stacking interactions are by far the well-studied interactions[8-12].These interactions are employed to control the conformational and topological features of the molecular assembly in the solid state[13-19]. More recently,these studies have been extended to unconventional hydrogen bonds where there are unusually short H…H contacts typically in the range from 0.17 to 0.24 nm[20-31].Several examples are known involving X-Hδ+…Hδ--Y interactions,such as B-H…H-N interactions[22]and Ga-H…H-N bonding[24],and X-Hδ+…Hδ+-Y interactions,such as C-H…H-C interactions[28].Herein,we report the syntheses and structures of two Pd(II)compounds containing furan-3-one ligands,which are stabilized by the weak interactions.The combination of C-H…O interactions and C-H…H-C interactions generates molecules forming a 3D network in 1,while the combination of C-H…H-C interactions and C-H…C interactions links molecules forming a 2D layered framework in 2.

1　Experimental

1.1Materials and measurements

All chemicals used were of analytical grade.The solvents were purified by conventional methods.C,H and N were determined using an Elementar vario EL elemental analyzer.The IR spectra were recorded on a Nicolet-AVATAR 360 FT-IR spectrometer using KBr pellets in the 4 000～400 cm-1regions.1H NMR spectra were recorded on a Varian 500 Bruker spectrometer.X-ray measurements were made on a Bruker Smart 1000 CCD diffractometer with graphite monochromated Mo Kα(λ=0.071 073 nm)radiation. UV-visible spectra were measured using a GBC Cintra 10e UV-visible spectrophotometer in CH3OH solution. The ligands L1and L2were prepared according to the literature[32]and their structures were displayed in chart 1.

Chart 1 Structures of the ligands L1and L2

1.2Synthesis of the complex Pd(L1)2(1)

A solution of Pd(CH3COO)2(0.011 2 g,0.05 mmol) in tetrahydrofuran(4 mL)was added dropwise to 4 mL tetrahydrofuran solution of L1(0.025 8 g,0.1 mmol). After heating for a while,4 mL CH3CN was added to the solution.The resulting mixture was refluxed for 2 h,and then cooled to room temperature.Then the reaction mixture was filtered and the red block-shaped crystals of 1 were obtained from the filtrate at room temperature after a few days.Anal.Calcd.for C32H40N2O4Pd(%):C,61.55;H,6.44;N,4.52.Found(%):C, 61.68;H,6.47;N,4.50.IR(KBr pellet,cm-1),2 973(m), 2 924(w),1 608(s),1 518(m),1 500(s),1 485(m), 1 457(m),1 424(m),1 368(m),1 357(m),1 308(m), 1 262(w),1 219(m),1 186(w),1 174(w),1 139(m), 991(m)897(w),841(m),825(m).1H NMR(500 MHz, CD3OD):δ 0.85(s,6H,-C(CH3)2),1.33(s,6H,-C(CH3)2), 2.33(s,3H,Ar-CH3),6.88(s,1H,CH),7.04(d,J= 7.95 Hz,2H,Ar-H),7.14(d,J=7.95 Hz,2H,Ar-H).

1.3Synthesis of the complex Pd(L2)2(2)

Using a procedure similar to that described above,reaction of ligand L2with Pd(CH3COO)2afforded complex 2 as red block-shaped crystals.Anal.Calcd. for C32H40N2O4Pd(%):C,61.47;H,6.44;N,4.53. Found(%):C,61.68;H,6.47;N,4.50.IR(KBr pellet, cm-1):2 975(w),2 925(w),1 610(s),1 512(s),1 482 (m),1 456(m),1 422(w),1 360(m),1 305(m),1 263 (m),1 187(w),1 140(w),1 127(w),992(w).1H NMR (500 MHz,CD3OD):δ 0.87(s,6H,-C(CH3)2),1.36(s, 6H,-C(CH3)2),2.36(s,3H,Ar-CH3),7.14(s,1H,CH), 6.93(t,J=8.10 Hz,1H,Ar-H),7.04(m,2H,Ar-H), 7.19(d,J=8.05 Hz,1H,Ar-H).

1.4X-ray crystallographic study

Crystallographic data of complexes 1～2 were collected on a Rapid-AUTO diffractometer and a Bruker SMART 1000 CCD diffractometer with graphite monochromatized Mo Kα radiation(λ=0.071 073 nm),respectively.ABSCOR-empirical absorption corrections were based on Fourier series approximation.The structures were solved by direct methods and refined by full-matrix least-squares on F2using the SHELXS-97 and SHELXL-97 programs[33].All non-hydrogen atoms were refined anisotropically.H atoms bound to C were placed in calculated positions and allowed to ride at distances of 0.093 nm(CH aromatic),0.096 nm(CH3)and 0.097 nm(CH2).The crystallography details for complexes 1 and 2 are presented in Table 1.Selected bond lengths and angles for complexes 1 and 2 are listed in Table2and 3.

CCDC:289373,1;629001,2.

Table1　Crystal data and structure refinement parameters for complexes 1～2

Table2　Selected bond lengths(nm)and bond angles(°)for 1

Continued Table 2

Table3　Selected bond lengths(nm)and bond angles(°)for 2

2　Results and discussion

2.1Structure description of Pd(L1)2(1)

Complex 1 crystallizes in the triclinic system, space group P1.The asymmetric unit contains two independent molecules.Both molecules(A and B) have similar conformations.In each molecule,two(L1)-ligands chelate to the Pd(Ⅱ)ion through their N and O donors,giving a four-coordinated Pd(Ⅱ)center with a trans-N2O2donor set.The coordination geometry at Pd(Ⅱ)is square-planar,with standard values for the distances from the metal ion to the coordinated atoms(Pd1-N1:0.203 0(2),Pd1-O1:0.199 2(2)nm for molecule A;Pd2-N2:0.203 1(2),Pd2-O3:0.199 12(18) nm for molecule B)(Fig.1).The six-membered chelate ring has a bite angle N-Pd-O of 93.58(9)°and 93.46(8)° for molecule A and B,respectively.The phenyl ring is almost perpendicular to the molecule plane:thedihedral angles between the phenyl ring and the PdN2O2plane is 88.0(5)°for molecule A and 86.2(5)° for molecule B.The furan ring is nearly coplanar with the molecule plane:the dihedral angles between the furan ring and PdN2O2plane is 2.6(4)°for molecule A and 0.5(4)°for molecule B.The angles between the furan ring and the methyl groups are 88.7(11)°for C2/ C3/C4 and 89.7(11)°for C5/C6/C7 in molecule A,and 89.9(10)°for C21/C22/C23 and 89.8(9)°for C18/C19/ C20 in molecule B.

Fig.1　Asymmetric structure unit of 1

Table4　Geometrical parameters of weak interactions in 1 and 2

In the molecule A,there are weak C-H…O hydrogen bonding interactions between the furan O atom and methyl H atom of phenyl ring(C16-H16B…O2 0.356 0 nm,Table 4),which bridge molecules forming an infinite chain along the c axis(Fig.2).In the molecule B,there are weak C-H…H-C interactions between the methyl H atom of phenyl ring and methyl H atom of furan ring(C22-H22A…H32B-C32,H22A…H32B 0.239 8 nm),which connect molecules giving rise to an infinite chain along the b axis.In addition,there are weak interaction(C30-H30…8B-C8,H30…H8B 0.223 3 nm,C5-H5…C31 0.373 0 nm,H5…C31 0.283 8 nm)between molecule A and molecule B,which further interconnect molecules resulting in a 3D network(Fig.3).

Fig.2　View of the 1D chain of 1 viewed along the c axis

2.2Structure description of Pd(L2)2(2)

Complex 2 crystallizes in the triclinic system, space group P1.Similar to complex 1,the asymmetric unit of 2 contains two independent molecules(C and D).The Pd(Ⅱ)ion center is coordinated by a N2O2donor set provided by two(L2)-ligands in transposition to complete the coordination sphere(Fig.4).

Fig.3　View of the 3D network of 1 viewed down the c axis

The coordination geometry at Pd(Ⅱ)is squareplanar,with standard values for the distances from the metal ion to the coordinated atoms(Pd1-N1 0.202 9(7) nm,Pd1-O1 0.198 0(5)nm for molecule C;Pd2-N2 0.202 1(6)nm,Pd2-O3 0.197 5(5)nm for molecule D). The six-membered chelate ring has a bite angle(N-Pd-O)of 94.3(2)°and 94.1(2)°for molecule C and D, respectively.The dihedral angles between the phenyl ring and the PdN2O2plane are 75.75(15)°and 69.38(11)° for molecule C and D,respectively,which are smaller than those observed in complex 1.The dihedral angles between the furan ring and PdN2O2plane are 3.25(16)° and 2.98(19)°for molecule C and D,respectively, which are larger than those observed in complex 1. The angles between the furan ring and the methyl groups are 89.6(3)°for C4/C8/C9 and 89.8(4)°for C1/ C6/C7 in molecule C,and 89.1(5)°for C17/C22/C23 and 89.8(4)°for C20/C24/C25 in molecule D.These values are similar to those observed in complex 1.

Compared with the complex 1,no C-H…O hydrogen bonding interactions were found between the furan O atom and methyl H atom of phenyl ring in complex 2.In molecule D,weak interactions between the methyl H atom of furan ring and phenyl H atom (C20-H20A…H29-C29,H20A…H29 0.2357 nm), link molecules forming an infinite chain along the b axis,which is further held together with molecule C via the weak interactions(C32-H32A…H6C-C6, H32A…C 0.236 1 nm,C16-H16C…C27 0.361 5 nm, H16C…C27 0.285 5 nm,Table 4),giving rise to a 2D layered framework(Fig.5).

Fig.4　Asymmetric structure unit of 2

The average Pd-O bond distances are 0.199 16 nm in 1 and 0.197 75 nm in 2.The average Pd-N bond distances in 1 and 2 are 0.203 05 and 0.202 45 nm,respectively.These values are within the range of those observed for other 4-coordinated Pd(Ⅱ)complexes with ligands containing O and N atoms[34-37].In complexes 1 and 2,the distribution of the bond lengths over the fragments N-C-C-C-O of the six-membered chelate ring indicates significant delocalization of the electron density.Similar structure has been reported in the Pd(Ⅱ)complex with 3-(1-aminoethylidene)-2H-chromene-2,4(3H)-dione[34].

Fig.5　View of the 2D layered framework of 2 viewed down the a axis

2.3IR,UV-Vis and1H NMR spectra

The IR spectra of the two ligands and the two complexes provide information about the metal-ligand bonding.The presence of one broad bands in 3 291 cm-1for L1and 3 304 cm-1for L2are assigned to N-H stretching vibrations.The bands in complexes 1 and 2 disappear,which suggest deprotonation of the N atoms of ligands.The strong absorption bands at 1 686,1 664, 1 604,15 59 cm-1for L1,1 662,1 616,1 593,1 577 cm-1for L2are due to C=C-C=O vibrations.The bands are shifted to lower wave numbers at 1 608 cm-1in 1 and 1 610 cm-1in 2,respectively,what can be attributed to the coordination of the O and N atoms to Pd (II)and indicate delocalization of the N-C-C-C-O sixmembered chelate ring.This phenomenon is in agreement with the results from the X-ray analysis.

The1H NMR spectra of complexes 1 and 2 in CD3OD are given in the experimental section.Complex 1 shows the signals of Hphenyl(δ 7.04 and 7.14)and Holefinic(δ 6.88)at the higher fields compared to the free ligand L1(Hphenyl:δ 7.13 and 7.20;Holefinic:δ 7.64). The peaks of the complex 2 are considerably shifted toward high-fields with respect to the peaks of the freeligand L2.The chemical shifts for signals of H atoms in complexes compared to ligands testify the coordination of the ligands with Pd(Ⅱ).

The UV-Vis spectral data for the two ligands and the two complexes were studied in CH3OH solvent (Fig.6).There are essentially two bands centered at 225 and 370 nm for L1,235 and 362 nm for L2, respectively,which correspond to intraligand π→π* transitions.In comparison with the two bands for L1and L2,the longer wavelength band for complex 1 and complex 2 remain the same energy,whereas the shorter wavelength band,appearing as a broad shoulder in the spectrum,shifts toward higher energy. All these phenomena account for the coordination of the ligands to Pd(Ⅱ).

Fig.6　UV-Vis spectra of L1,L2(2.4×10-5mol·L-1),and complexes 1～2(5.8×10-6mol·L-1)in CH3OH

3　Conclusions

In this work,two Pd(Ⅱ)complexes were prepared in high yield under refluxing in the mixed solution of THF and CH3CN for 2 h.Their structures were characterized by elemental analyses,IR spectra,1H NMR spectra,UV-Vis spectral and single-crystal X-ray diffraction.The asymmetric units of both the compounds 1 and 2 contain two independent molecules. The ligands are found to bind the Pd(Ⅱ)via their N and O donors giving a four-coordinate Pd(Ⅱ)center with a trans-N2O2donor set.In 1,the molecules A form 1D chains through hydrogen bonds along the c axis and the molecules B form 1D chains via weak hydrogen bonds along the b axis,molecules A and B are further extended through the weak interactions into a 3D networks.In 2,the weak interactions in molecules D link molecules forming an infinite chain along the b axis,which are further interlinked to molecules C via unconventional hydrogen bonds into a 2D layered framework.

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Syntheses,Crystal Structures and Spectral Properties of Two Pd(Ⅱ)Complexes Containing Furan-3-one Ligands

ZHAO Ming-Xia1XIONG Li-Qin2CAI Yong-Le1CHANG Jin3REN Hong-Yu3ZHANG Hua-Bei3QI Chuan-Min＊,3
(1Department of Mining Engineering,Shanxi Institute of Technology,Yangquan,Shanxi 045000,China)
(2School of Biomedical Engineering,Shanghai Jiao Tong University,Shanghai 200025,China)
(3Key Laboratory of Radiopharmaceuticals,Ministry of Education,College of Chemistry, Beijing Normal University,Beijing 100875,China)

Two compounds,Pd(L1)2(1)and Pd(L2)2(2)(L1=(Z)-4-((p-toluidino)methylene)-2,2,5,5-tetramethyldihydrofuran-3(2H)-one,L2=(Z)-4-((o-toluidino)methylene)-2,2,5,5-tetramethyl-dihydrofuran-3(2H)-one)),have been synthesized and characterized by elemental analyses,IR spectra,1H NMR spectra,UV-Vis spectral and singlecrystal X-ray diffraction.The crystal structures of compounds are shown to contain a variety of weak interactions. In 1,the C-H…O interactions between the furan O atom and methyl H atom of phenyl ring bridge molecules forming an infinite chain along the c axis,which is interconnected via the weak C-H…H-C interactions and CH…C interactions,giving rise to a 3D network.In 2,molecules are held together by weak C-H…H-C interactions and C-H…C interactions into a 2D layered framework.CCDC:289373,1;629001,2.

syntheses;Pd(Ⅱ);furan-3-one;crystal structure;weak interactionsntroduction

O614.82+3

A

1001-4861(2016)11-2017-08

10.11862/CJIC.2016.220

2016-01-09。收修改稿日期：2016-08-08。

國家自然科學基金(No.230100075)和國家科技支撐(No.2014BAA03B03)項目資助。＊通信聯系人。E-mail：qicmin@sohu.com