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    三角柔性多羧酸金屬有機骨架化合物的合成、結(jié)構(gòu)及熒光性質(zhì)

    2018-12-10 06:49:22榮介偉章文偉
    無機化學(xué)學(xué)報 2018年12期
    關(guān)鍵詞:化工學(xué)院南京大學(xué)淮南

    榮介偉 章文偉

    (1淮南師范學(xué)院化學(xué)與材料工程學(xué)院,淮南 232038)

    (2南京大學(xué)化學(xué)化工學(xué)院,配位化學(xué)國家重點實驗室,南京 210023)

    0 Introduction

    Over the past two decades,the metal-organic frameworks (MOFs)have received growing interest not only for their bewitching architectures[1-2],but also for their potential applications in gas adsorption[3-5],magnetism[6],catalysis[7-9],nonlinear optics[10-11]and luminescence[12-15].Moreover,with respect to conventional metal-organic frameworks,luminescent MOFs have distinctive advantages owing to their widely potential applications such as light-emitting diodes,environmental probe,display devices,electro-chemical sensors and biomedicine[16].Photoluminescent property in MOFs commonly causes by the organic building components such as conjugated organic ligands and inorganic metal ions clusters with closed shell electron configuration[17].

    Among various conjugated organic ligands,owing to their natural characteristics,the tripodal rigid carboxylate ligands are promising candidates for constructing porous MOFs because of their abundant coordination modes to metal ions,allowing for various structural topologies[18-19].Recently,triangle flexible carboxylate ligands were used to build interesting metal-organic frameworks[20-21],the flexibility of the triangle flexible carboxylate ligands provides the constructed functional MOFs tunable structures,which further affects the properties[22-23].Moreover,when the ancillary bridging pyridine linker is introduced to build the frameworks,the final structures have greater tenability because of its great effects on the final architectures and topology as well as coordination modes and molecular conformations of carboxylate acids[24-27].Although a lot of transition metal ions have been used to construct MOFs,the Zn-based MOFs are the most interested transition metal-based luminescent MOFs.MOFs based on d10metal ions not only have various coordination geometries,but also display excellent luminescence behaviour with functionalπconjugated aromatic ligands[28-29].

    Herein,we selected the triangle flexible multicarboxylic acid,namely,1,3,5-tri(4-carboxyphenoxy)benzene ligand (H3TCPB),and an ancillary bridging pyridine linker,namely,4,4′-bipyridine (4,4′-BPY)to synthesize two new metal-organic frameworks{[Zn3(TCPB)2(4,4′-BPY)]·DMF·3H2O}n(1)with trinuclear zinc cluster units and{[Co1.5(TCPB)(DMF)(H2O)]·DMF}n(2)with trinuclear cobalt cluster SBUs,and studied their crystal structures and photoluminescent properties in detail.

    1 Experimental

    1.1 Materials and measurements

    All reagents and materials are of analytical grade and used as received from commercial sources without further purification.The ligand 1,3,5-tri(4-carboxyphenoxy)benzene ligand (H3TCPB)was prepared according to the literature procedure[30].Elemental analyses(C,H and N)were carried out on a Perkin-Elmer 240 analyzer.The IR spectra were obtained on a NICOLET iS10 spectrometer in the 4 000~500 cm-1region.Powder X-ray diffraction (PXRD)measurements using Cu Kα (λ=0.154 056 nm)radiation at roomtemperature(40 kV,40 mA,Scanning rang:5°~50°)were carried out in air with a Bruker D8 Discover diffractometer.Thermal gravimetric analyses (TGA)were performed using a DTA-TGA 2960 thermogravimetric analyzer in nitrogen atmosphere with a heating rate of 10℃·min-1from 30 to 700℃.The luminescence spectra in the solid states were performed on RF-5301 PC fluorescence spectrometer at room temperature.

    1.2 Synthesis

    1.2.1 Synthesis of complex{[Zn3(TCPB)2(4,4′-BPY)]·DMF·3H2O}n(1)

    A solution of Zn(NO3)3·6H2O (6 mg,0.02 mmol),H3TCPB (5 mg,0.01 mmol),4,4′-BPY (2 mg,0.013 mmol),DMF (0.5 mL)and H2O (0.1 mL)were mixed and sealed in a 10 mL Teflon-lined autoclave and heated to 85℃for 48 h.Colorless block-shaped crystals were obtained after gradually cooled to room temperature at a rate of 10 ℃·h-1(Yield:75%based on Zn).Anal.Calcd.for C67H51Zn3N3O22(%):C,55.64;H,3.55;N,2.91.Found(%):C,55.45;H,3.43;N,2.63.Selected IR data (KBr pellet,cm-1):3 392 (b),3 071(w),1 595 (s),1 397 (s),1 223 (s),1 161 (s),1 117 (s),1 005 (s),855 (m),782 (s),708 (m),645 (m)(Supporting Information,Fig.S1).

    1.2.2 Synthesis of complex{[Co1.5(TCPB)(DMF)(H2O)]·DMF}n(2)

    A solution of Co(NO3)2·6H2O (6 mg,0.02 mmol),H3TCPB (5 mg,0.01 mmol),DMF (0.4 mL)and H2O(0.1 mL)were mixed and sealed in a 10 mL Teflonlined autoclave and heated to 120℃for 48 h.Lightpink block-shaped crystals were obtained after gradually cooled to room temperature at a rate of 5℃·h-1(Yield:75%based on Co).Anal.Calcd.for C33H31Co1.5N2O12(%):C,53.85;H,4.25;N,3.81.Found(%):C,53.65;H,4.45;N,3.90.Selected IR data(KBr pellet,cm-1):3 427 (b),2 942 (w),1 677 (s),1 657 (s),1 631 (s),1 594 (s),1 412 (s),1 222 (s),1 161 (m),1 110(m),1 003 (m),791 (m)(Fig.S1).

    1.3 Single crystal X-ray crystallography

    Suitable single crystals of 1 and 2 were carefully selected under an optical microscope and glued to thin glass fibers.Single crystal X-ray diffraction data were collected on a Bruker Smart ApexⅡCCD diffractometer at 296 K using graphite monochromated Mo Kα radiation (λ=0.071 073 nm).Data reductions and absorption corrections were performed with the SAINT[31]and SADABS2[32]software packages,respectively.Structure was solved by a direct method using the SHELXL-97 software package[33].The non-hydrogen atoms were anisotropically refined using the fullmatrix least-squares method on F2.All hydrogen atoms were placed at the calculated positions and refined riding on the parent atoms.In complex 1,solvent molecules in the structure were highly disordered and were impossible to refine using conventional discreteatom models.To resolve this issue,the contribution of solvent electron density was removed by SQUEEZE routine in PLATON[34].

    The crystallographic data and details of structural refinements for 1 and 2 are listed in Table 1 and selected bond distances and angles are summarized in Table S1 and Table S2.

    CCDC:1860924,1;1865905,2.

    Table 1 Crystallographic data and structural refinements for 1 and 2

    2 Results and discussion

    2.1 Crystal structures

    The powder X-ray diffraction (PXRD)experiments for complexes 1 and 2 were carried out carefully to check phase purity at room temperature.The patterns showed that the main peaks of the synthesized MOFs were closely consistent with those of the simulations from the single-crystal X-ray diffraction data,which imply high quality of the obtained products (Fig.S2).Crystal of 1 belongs to the triclinic space group P1.As shown in Fig.1a,its asymmetric unit cell consists of thee Zn2+ions,two fully deprotonated TCPB3-ligands and one coordinated 4,4′-BPY molecule.Three crystallographically independent Zn2+ions(labeled as Zn1,Zn2 and Zn3,respectively)are coordinated with oxygen atoms and nitrogen atom,exhibiting three different coordination geometries (Fig.1b).The Zn1…Zn2 distance is about 0.324 10(2)nm and the Zn1…Zn3 distance is about 0.325 90(2)nm.The Zn1 atom was located in the center and bridged Zn2 and Zn3 atoms to form a trinuclear Zn cluster unit (Fig.1c).The Zn1 ion in the middle of the[Zn3(CO2)6]SBU is octahedron coordination geometry,encircled by six carboxylate oxygen atoms (O2a,O5c,O8d,O11e,O15 and O18b)from six different TCPB3-ligands to result in a[Zn1O6]unit,while the other two asymmetry-related Zn2 and Zn3 ions both adopt a distorted trigonal bipyramid coordination geometry with a [Zn2O4N]and[Zn3O4N]unit,respectively (Fig.1b and Fig.S3),coordinated by four carboxylate oxygen atoms(O10,O14g,O17f and O18f for Zn2;O1,O5h,O6h and O9e for Zn3)from three different TCPB3-ligands,one nitrogen atom from the coordinated 4,4′-BPY molecule (N2 for Zn2;N1 for Zn3).The carboxylate groups in complex 1 adopt two kinds of coordination modes.One shows chelating and bridging modes to link two Zn ions,while the other two adopt a bidentate bridging coordination mode to coordinate with two Zn ions.The dihedral angles between the central benzene (A)and the three benzene rings B,C and D are 75.839°,69.199°and 69.139°,respectively,and the dihedral angles among the three benzene rings B and C,B and D,and C and D are 78.830°,39.346°and 72.518°,respectively(Fig.1c).This dihedral data indicates that ligand TCPB3-is extremely unsymmetrical.The dihedral angle between the two pyridyl rings is 30.961°.Therefore,two pyridyl rings of 4,4′-BPY are not coplanar.In 1,each TCPB3-ligand links three[Zn3(CO2)6]SBUs (Fig.1c),each[Zn3(CO2)6]SBU is connected by six TCPB3-ligands and two 4,4′-BPY ligands,and each 4,4′-BPY ligand links two[Zn3(CO2)6]SBUs by terminal nitrogen atoms (Fig.1d),such building units are repeated to form a three-dimensioal(3D)network.As summarized in Table S1,the Zn-O bond lengths range from 0.193 5(2)to 0.232 1(3)nm,the bond distances of Zn-N are in the range of 0.202 4(3)~0.204 4(3)nm,and the O-Zn-O bond angles span from 56.97°to 179.37°,thecoordination bond lengthsand bond angles around the Zn ions are in good agreement with the reports[35].

    Fig.1 (a)Coordination environments of Zn2+ions with the H atoms omitted for clarity;(b)Coordination polyhedron of Zn2+ions;(c)One TCPB3-ligand linking three[Zn3(CO2)6]SBUs;(d)One[Zn3(CO2)6]SBU connected by six TCPB3-ligands and two 4,4′-BPY linkers

    The guest DMF and water molecules,being disordered,locate in the channels.All DMF and water molecules can be completely removed upon heating,and there exist two types of one-dimensional channels along the c axis,which possess the open window of 1.205(2)nm×0.860(3)nm (A)and 1.815(3)nm×1.760(3)nm (B)when the van der Waals radii of the atoms at the wall of the channel are subtracted,respectively (Fig.2c).Moreover,open channel systems also exist along the a and b axis,with an open window size of 1.775(2)nm×1.576(2)nm and 1.441(2)nm×1.350(3)nm,respectively (Fig.2a and 2b),and the solvent-accessible volume is about 46.2%calculated by PLATON/SOLV[34]when the guest DMF and water molecules are removed (Fig.2 and Fig.S3).as Co1 and Co2,respectively)exhibit different coordination geometries although they are both coordinated with six oxygen atoms (Fig.4b).The coordination geometry around Co1 ions can be described as an octahedron with its six coordinated oxygen atoms coming from six different TCPB3-ligands(O4,O4c,O7b,O7e,O8a and O8d),which results in a [Co1O6]unit.As for Co2 ions,they bond to four oxygen atoms (O5a,O6f,O7f and O9)from three TCPB3-ligands,one oxygen atom (O10)from one DMF molecule and one oxygen atom (O11)from one H2O molecule with a [Co2O6]unit,resulting in distorted octahedron geometries.As shown in Fig.4c and 4d,amongthesix coordinated TCPB3-ligands,four carboxylates from four TCPB3-coordinate to Co1 and Co2 as a bidentate bridging coordination mode,while the other two carboxylates from two different TCPB3-ligands coordinate to Co1 and Co2 centers in a chelating and bridging coordination mode to give a three-nuclear[Co3(COO)6]subunit (SBU)with Co1 …Co2 distance of 0.351 3(2)nm within this SBU.The dihedral angles between the central phenyl ring (A)and the three phenyl rings B,C and D are 70.93°,73.73°and 80.89°,respectively,and the dihedral angles among the three phenyl rings B and C,B and D,and C and D are 80.00°,49.44°and 35.55°,respectively (Fig.4c).These dihedral data indicate that the TCPB3-ligand is extremely unsymmetrical and the phenyl rings in TCPB3-are not coplanar so as to satisfy the coordination geometry of Co2+.The bond lengths of Co-O bond distances range from 0.202 78(16)to 0.221 48 (16)nm,and the O-Co-O bond angles span from 60.16° to 177.02° (Table S2),which are compatible with the values of the previously published reports in literatures[36].The carboxylate groups in complex 2 adopt chelating and bidentate bridging coordination modes to coordinate with three Co ions to form a three-nuclear Co cluster unit[Co3(COO)6]SBU.Overall,as shown in Fig.4c and 4d,each TCPB3-ligand connects three[Co3(COO)6]SBUs and each[Co3(COO)6]SBU is surrounded by six TCPB3-ligands,generating a two-dimensional (2D)net-like layered framework (Fig.4e and S4).From the view point of topology,the 2D structure of 2 can be described as a(3,6)-connected network with Schlfli symbol of{43}4·{46·618·84}by considering each[Co3(COO)6]SBU as a 6-connected node and the organic ligand TCPB3-as a 3-connected node (Fig.2f).

    Fig.2 Space filled representation of the 3D framework in 1 viewed from a,b,and c directions

    Fig.3 (3,8)-connected network of 1

    Fig.4 (a)Coordination environments of Co2+ions with the H atoms omitted for clarity;(b)Coordination polyhedron of Co2+ions;(c)One TCPB3-ligand linking three[Co3(COO)6]SBUs;(d)One[Co3(COO)6]SBU connected by six TCPB3-ligands;(e)Polyhedral representation of 2 viewed from a direction;(f)(3,6)-connected network of 2

    2.2 Thermal analysis

    The thermal stability of 1 and 2 were also detected via thermogravimetric analyses (TGA).The thermal analyses of powdered samples of 1 and 2 were performed under a nitrogen atmosphere.As shown in Fig.5,complex 1 lost three guest water molecules and one guest DMF molecule from room temperature to 200 ℃ (Obsd.9.11%,Calcd.8.78%),while complex 2 was stable up to 105℃and then exhibited one step of weight loss.The weight loss of 22.11%(Calcd.22.28%)in the temperature range of 105~210 ℃corresponds to the release of one guest DMF molecule,one coordinated DMF molecule and one coordinated water molecule.After the guest and the coordinated solvent molecules are removed,a plateau appears and the desolvated sample was thermally stable up to 290℃for 1 and 450℃for 2.Above 290℃for 1 and 450℃for 2,the framework gradually began to break down with the decomposition of the organic part of framework.From the decomposition temperature shown above,complex 2 exhibits good thermal stability.This may be attributed to the coordinatively linked net-like structure.

    Fig.5 TG curves of 1 and 2

    2.3 Photoluminescence property

    The solid-state photoluminescent properties of complex 1 and 2 together with H3TCPB and 4,4′-BPY were investigated at room temperature.As depicted in Fig.6,the H3TCPB ligand exhibited only a broad emission band with a maximum at 354 nm upon excitation with λex=280 nm (the excitation spectra is presented in Fig.S5),and 4,4′-bipyridine ligand showed an intense band centered at 466 nm,together with a broad and weak emission band located around 361 nm under the excitation at 300 nm,which may be caused by the π*-π and π*-n transition.As for complex 1,upon excitation at 320 nm,it showed blue luminescence (Fig.7)with a large broad band emission centered at 465 nm and a weak emission at 361 nm(Fig.6,and the excitation spectra is given in Fig.S6).As the literature reported,the d10configured Znギcations are electrochemically inert,therefore,when coordinated by ligands,they cannot take an electron from the ligand with their 3d-orbitals,nor donate an electron to the ligand[37].In contrast to the emission of the free ligands,the emission band of 1 exhibited redshifted as compared to free H3TCPB ligand,and was close to the free 4,4′-BPY ligand,inferring that its emission bands may be assigned to the intra-ligand charge transfer (ILCT),neither metal-to-ligand charge transfer (MLCT)nor ligand-to-metal charge transfer(LMCT)happened[38].Moreover,the red-shift of the intense emission in 1 could be attributed to the coordination effect,which affects the HOMO and LUMO levels of the ligand to change the transition energy,and enables the rigidity of the aromatic backbones and reduces the loss of energy by radiationless decay of the intraligand emissions[39].However,experimental results showed that complex 2 was nonemissive under similar conditions,indicating that the emissions of organic ligands may be quenched completely in the complex,which may be due to the emission quencher of Coギin the structure[38].

    Fig.6 Emission spectra of 1,4,4′-BPY and H3TCPB ligand in solid state at room temperature

    Fig.7 CIEchromaticity diagram for 1

    3 Conclusions

    In summary,two novel MOFs,{[Zn3(TCPB)2(4,4′-BPY)]·DMF·3H2O}n(1)and{[Co1.5(TCPB)(DMF)(H2O)]·DMF}n(2) (H3TCPB=1,3,5-tri(4-carboxyphenoxy)benzene),have been successfully synthesized via solvothermal reactions.Complex 1 possesses a threedimensional net framework constructed by threenuclear zinc SBUs,TCPB3-and 4,4′-BPY linker.Complex 2 has a 2D layered structure constructed by trinuclear cobalt cluster as SBUs.The solid-state photoluminescent property of 1 was investigated,and the emission band was assigned to the intra-ligand charge transfer (ILCT).

    Acknowledgments:The authors thank National Nature Science Foundation of China for financial support(Grants No.21371091,21371150).

    Supportinginformation isavailableat http://www.wjhxxb.cn

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