Syntheses,Characterization and Fluorescence Properties Analysis of Two Lanthanide Coordination Polymers Based on Axial Chirality Ligand 2,2′-Dinitro-4,4′-biphenyldicarboxylic Acid

JI QinCHEN Li-Zhuang

(School of Environmental and Chemical Engineering,Jiangsu University of Science and Technology,Zhenjiang,Jiangsu 212003,China)

Syntheses,Characterization and Fluorescence Properties Analysis of Two Lanthanide Coordination Polymers Based on Axial Chirality Ligand 2,2′-Dinitro-4,4′-biphenyldicarboxylic Acid

JI QinCHEN Li-Zhuang＊

(School of Environmental and Chemical Engineering,Jiangsu University of Science and Technology,Zhenjiang,Jiangsu 212003,China)

Two lanthanide coordination polymers,La(nbpdc)(phen)(FA)(1),Eu(nbpdc)(phen)(FA)(2)(FA=formic acid ion)based on bridging ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid(H2nbpdc)and 1,10-Phenanthroline monohydrate(phen),have been synthesized by the hydrothermal method and characterized by IR,single-crystal X-ray structure analysis,thermogravimetric analysis,luminescent properties,circular dichroism(CD)analysis and dielectric properties.Complexes 1 and 2 exhibited a rare three-interlude 3D structure with the same topology structure of(44·62).In addition,the two complexes exhibit fluorescent emissions in the solid state at room temperature. Fluorescent analysis of complexes 1 and 2 showed an intense emission band at 606 nm(λex=495 nm)and 615.5 nm (λex=395.5 nm),respectively.Moreover,the circular dichroism analysis of complexes 1 and 2 was measured with chirality.CCDC:1504875,1;1504877,2.

coordination polymer;hydrothermal condition;fluorescence;chirality

Coordination polymers have received attention because of the intriguing structures and potential applications in magnetism,catalysis,luminescence, conductivity,sensors,porosity,nonlinear optics,etc[1-18]. Luminescentlanthanidecomplexeshavebeen extensively studied due to extremely narrow emission bands,large Stokes shift,long luminescence decay times,and no theoretical cap on quantum efficiency; particularly,europium,terbium,samarium,and dysprosium have interesting luminescent properties, such as red emission for Euion.They are very attractive for applications in light-emitting diodes[19], laser materials[20],and as probes and labels in a variety of biological and chemical applications[21-22].Luminescent intensities of lanthanide complexes are dependent on the ligands.In our continuing effort in this field[23-24], we chose ligand 2,2′-dinitro-4,4′-biphenyldicarboxylic acid(H2nbpdc)as an organic building block in an attempt to construct coordination polymers with new structural features.In addition,the two benzoate moieties in nbpdc twist freely due to two nitro groups, thus bringing about an organic building block which is geometrically different from the mother ligand and hence may lead to different topologies.Moreover, nbpdc ligand may induce cluster aggrega-tion and link the clusters into extended networks.However,to the best of our knowledge,frameworks based on ligand nbpdc have rarely been studied[25].Herein,we report thesynthesis,crystalstructure,andluminescent properties of two lanthanidecomplexes.

1 Experimental

1.1 Materials and physical measurements

All of the chemicals and solvents except for nbpdc ligand in this study obtained from Shanghai Jingchun Scientific Company were of reagent grade and used without any further purification.The nbpdc ligand was prepared by the method reported previously[26].Infrared spectra were recorded on a SHIMADZU IRprestige-21FTIR-8400Sspectrometerinthe spectral range of 4000～500 cm-1with samples in the form of potassium bromide pellets.Elemental analyses were taken on a Perkin-Elmer 240C elemental analyzer. The solid-state fluorescent spectra were recorded by Spectrofluorometer FS5 at room temperature.Thermogravimetric analyses(TGA)were conducted on a NETZSCH TG 209 F3 thermo gravimeter with the heating rate of 10 K·min-1in a N2atmosphere.The chirality of complexes was characterized by JASCO J-1500 circular dichroism.

1.2 Preparation of complex 1

H2nbpdc(0.1 mmol,0.033 0 g),phen(0.1 mmol, 0.019 8 g)and La(NO3)3(0.1 mmol,0.043 3 g)were placed in a 25 mL Teflon-lined stainless-steel vessel. After the addition of water(1.5 mL)and DMF(1.5 mL),the solution was heated to 125℃for three days. Afterwards,the reaction system was slowly cooled down(a descent rate of 5℃·h-1)to room temperature. Colorless transparent bulk crystals were obtained, washed with distilled water,and dried in air.Yield: 64%(based on nbpdc).Anal.Calcd.(%)for C27H14N4O10La:C,46.73;H,2.01;N,8.08.Found(%):C,45.47; H,1.96;N,7.39.IR data(KBr pellet,cm-1)(Fig.S1): 3 402(w),3 090(w),2 922(w),2 838(w),1 599(s), 1 515(m),1 396(s),1 335(s),1 094(w),913(w),842 (m),770(s),710(m),517(w).

1.3 Preparation of complex 2

The synthesis of 2 was similar with 1 except that Eu(NO3)3(0.1 mmol,0.044 6 g)was used instead of La(NO3)3.Colorless block crystals were obtained in 52%yield.Anal.Calcd.(%)for C27H15N4O10Eu:C,45.80; H,2.12;N,7.92.Found(%):C,44.93;H,2.03;N, 6.46.IR data(KBr pellet,cm-1)(Fig.S2):3 402(s), 3 086(m),2 948(w),2 855(w),1 652(w),1 596(w),1 523 (s),1 403(s),1 338(m),1 078(m),995(w),912(m),839 (s),773(s),719(s),624(m).

1.4 Single-crystal X-ray diffraction

Single crystals of 1 and 2 with appropriate dimensions(0.26 mm×0.30 mm×0.24 mm for 1,0.30 mm× 0.30 mm×0.20 mm for 2)were selected for data collection on a Rigaku SCXmini diffractometer equipped with a graphite-monochromated Mo Kα radiation(λ= 0.071 073 nm),using an ω scan mode at 296 K.The absorption correction was carried out by a multi-scan method.The structures were solved by direct methods with SHELXS-97 and refined by full-matrix least-squares on F2with SHELXL-97[27-28].While H atoms were located in calculated positions and refined using a riding model,which were found by electron cloud density.Somedisorderedsolventmoleculeswere treated by SQUEEZE[29]process.Topology information for complexes 1～2 was obtained using TOPOS 4.0[30]. All non-hydrogen atoms were refined with anisotropic thermal parameters.All hydrogen atoms attached to C, N and O atoms were added theoretically and refined with a riding model and fixed isotropic thermal parameters.Detailed data collection and refinement of complexes 1 and 2 are summarized in Table 1,and the selected bond distances and bond angles of 1 and 2 are listed in Table 2 and 3,respectively.

CCDC:1504875,1;1504877,2.

Table 1Data collection and processing parameters for 1 and 2

Table 2Selected bond lengths(nm)and bond angles(°)of 1

Table 3Selected bond lengths(nm)and bond angles(°)of 2

1.5 Dielectric measurements

The temperature dependences of the dielectric constants of two complexes were measured on the Tonghui TH2828A analyzer in the temperature ranges of 120～290 K and 150～230 K,respectively,within the frequency range of 500 Hz to 1 MHz at the AC voltage of 1 V.Crystals of the two compounds with appropriate dimensions were prepared with silverconductive glue and used for dielectric studies.

2 Results and discussion

2.1 Crystal structures of 1 and 2

Single-crystalX-raydiffractionrevealsthat complexes 1 and 2 crystallize in the orthorhombic system,space group P212121and displays a 3D coordination framework.Complexes 1 and 2 are isostructural,so the crystal structure of 1 is described in detail.As shown in Fig.1a,the asymmetric unit of crystal 1 contains one Laion,one nbpdc ligand, one phen and one formic acid ion(FA).Besides,the Lais in a slightly distorted dodecahedral environment.Moreover,it is interesting that only ligand nbpdc coordinates metal Laion as a two-dimensional networkthatgraduallyformsathree-dimensional structure by coordinating phen and Laions(Fig.1b). To get a better insight into the structure of complex 1, topological analysis was conducted.Each 2-connected bridging nbpdc ligand can be regarded as a linear linker.Each phen ligand can also be treated as a 2-connector and each Laion can be regarded as 8-connected node since it links four nbpdc,one phen and two formic acid ions.Thus,the simplified overall structure of 1 is 4-connected uninodal net with stoichiometry(4-c),as shown in Fig.1c.The point(Schl?fli) symbol for net is(44,62)calculated by TOPOS program and the topological type is sql.

Fig.1(a)View of the coordination environment of Lain complex 1 with displacement ellipsoids drawn at the 50%probability level;(b)Three-dimensional structure of complex 1;(c)Topological analysis of complex 1

2.2 Thermogravimetric analysis

In order to investigate the thermal stability of complexes 1～2,TGA was performed in N2atmosphere. As shown in Fig.S3,the TGA curve of complex 1 display three weight loss steps.The first weight loss from 480 to 590℃is attributed to the loss of one formic acid ion(Obsd.6.7%,Calcd.6.3%).The second weight loss of 1 between 600 and 860℃perhaps results from the release of coordinated 1,10-Phenanthroline molecule(Obsd.26.5%,Calcd.25.9%). Upon heating,the framework decomposed at above 900℃.For the complex 2,the data display the first weight loss platform at above 500℃,corresponding to the release of one formic acid ion(Obsd.6.5%,Calcd. 6.2%).Upon temperature increase,the structure began to collapse slowly.

2.3 Luminescent properties

The luminescent properties of 1 and 2 in the solid state were investigated at room temperature.As shown in Fig.2,complex 1 exhibits maximal emission peaks at 606 nm(λex=495 nm),suggesting that 1 may be a good visible light-emitting material.The photoluminescentmechanismistentativelyattributedto ligand-to-ligandtransitions,beinginreasonable agreement with this kind of metal complexes.

Fig.2Solid state emission spectrum of 1

The fluorescence spectrum of 2 was evaluated in the solid state upon the excitation at 395.5 nm at room temperature showing the5D0→7F0(J=0～4)characteristic transitions of Eu.The strongest narrowband emission at 615.5 nm is characteristic of the hypersensitive5D0→7F1transition of Eu,which is more intense than the5D0→7F0transition at 591 nm,5D0→7F3transition at 688 nm and5D0→7F4transition at 697 nm.One weak emission bands at 649 nm correspond to5D0→7F2transitions(Fig.3).Intense red fluorescence for 2 is observed under UV excitation, suggestingthatithaspotentialapplicationin photoactive materials.

Fig.3Solid state emission spectrum of 2

2.4 Circular dichroism(CD)analysis

Fig.4Circular dichroism(CD)of H2nbpdc ligand using KBr pellets at room temperature

Fig.5Circular Dichroism(CD)of complex 1 using KBr pellets at room temperature

Fig.6Circular dichroism(CD)of complex 2 using KBr pellets at room temperature

AccordingtotheP212121spacegroupof complexes 1 and 2 and a chirality of H2nbpdc ligand (Fig.4),the study on the chirality of complexes 1 and 2 is conducted,respectively.As shown in Fig.5～6, compared with H2nbpdc,complexes 1 and 2 have appeared correspondingly higher positive peaks at a wavelength of about 220 nm,which can be regarded as the peak of the chiral ligands.In addition,the ligand appeared wide peak at 289 nm,and compared to complexes 1 and 2,it is expected that the peak of the complexes are similar to the peak of ligand.So it isfurtherprovedthatthecomplexeshavethe chirality.

2.5 Dielectric properties

Materials with temperature-dependent dielectric constants which rapidly fluctuate may have phase transition,piezoelectric,and ferroelectric properties. The permitivities(ε=ε1-iε2)of powdered samples of the two complexes as pellets were measured,where ε1and ε2are the corresponding real part and imaginary part of dielectric constant,respectively.

Inaddition,thedielectricconstantsoftwo complexes show similar temperature dependence(Fig. 7).The temperature-dependence dielectric constant at differentfrequencyindicatedthatthedielectric constants(ε1)gradually increase with a rise of temperature(160～280 K).

Fig.7Dielectric constants of complexes 1(a)and 2(b)from 160 to 280 K at different frequencies

3 Conclusions

Two metal-organic coordination polymers based on 2,2′-dinitro-4,4′-biphenyldicarboxylic acid were successfully synthesized under hydrothermal conditions and structurally characterized.Complexes 1 and 2 generated a 3D framework with(44,62)topologies. Furthermore,complexes 1 and 2 exhibited strong fluorescentemissioninthesolidstateatroom temperature.

Supporting information is available at http://www.wjhxxb.cn

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基于軸手性配體的兩個鑭系金屬配合物的合成、表征及其熒光性質

吉沁 陳立莊＊
(江蘇科技大學環境與化學工程學院，鎮江212003)

通過水熱法，合成了2個基于軸手性配體2，2′-dinitro-4，4′-biphenyldicarboxylic acid(H2nbpdc)的配位聚合物[La(nbpdc) (phen)(FA)]n(1)，[Eu(nbpdc)(phen)(FA)]n(2)(phen=菲咯啉，FA=甲酸根)，并且對2個化合物進行了紅外、單晶X射線衍射、熱重、熒光、CD譜及介電性質的研究。晶體結構測試表明，2個化合物結晶在正交晶系P212121手性空間群，且具有相同的三維拓撲結構。熒光性質測定表明化合物1和2分別在606和615.5 nm處有強的發射光譜。與此同時，固體CD譜測試進一步證實2個化合物具有手性。

配位聚合物；水熱反應；熒光；手性

O614.33+1；O614.33+8

A

1001-4861(2017)05-0874-07

2016-11-14。收修改稿日期：2017-03-09。

10.11862/CJIC.2017.099

國家自然科學基金(No.21671084)、江蘇省自然科學基金(No.BK20131244)、江蘇省“六大人才高峰”項目(No.2014-XCL-008)、江蘇省青藍工程項目、江蘇省高校研究生實踐創新計劃項目(No.KYLX16-0508)和江蘇教育廳基金(No.16KJB430011)資助。

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