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手性Eu(Ⅲ)配合物的合成和作为ct-DNA荧光探针的研究 被引量:2

Synthesis,Characterization of Chiral Eu(Ⅲ) Complexes and Study of Chiral Fluorescence Probe to ct-DNA
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摘要 通过制备拆分剂氯化(8S,9R)-(-)-N-苄基辛可尼定,拆分了外消旋联萘酚得到其两种对映异构体,以手性联萘酚为原料分别合成了配体(R)-L和(S)-L及其相应的Eu(Ⅲ)配合物(R or S)-L-Eu(NO3)3,并测定了旋光度。分别研究了配合物(R or S)-L-Eu(NO3)3与ct-DNA的作用方式及键合常数,发现配合物与小牛胸腺DNA(ct-DNA)存在插入作用,且(R)-L-Eu3+配合物与ct-DNA的键合能力较强。由于ct-DNA对(R)-L-Eu3+配合物荧光的增敏作用,选择(R)-L-Eu3+配合物作为ct-DNA的手性荧光探针,在最佳实验条件下,其线性范围为0.11×10-5~0.55×10-5 mol·L-1,0.55×10-5~7.8×10-5 mol·L-1,检出限为5.85×10-7 mol·L-1。 Prepared by splitting chloride (8S,9R)- (-)-N-benzyl Keesing Marconiset, resolution of the raeemic binaphthol by its two enantiomers, with chiral binaphthol as raw materials were synthesized (R)-L and (S)-L and Eu ( Ⅲ ) complexes, and their optical ro- tation values were measured. The interaction between ct-DNA and (R or S)-L-Eu( NO3 )3 was investigated, the results indicated that intercalation played an important role between ct-DNA and complexes. The binding constant of (R) -L-Eu ( NO3 ) s with ct-DNA was higher than that of (S)-L-Eu( NO3 )3. Because ct-DNA could obviously increase the fluorescent intensity of (R)-L-Eu3+ , (R)-L-Eu ( NO3 ) s was chosen as chiral fluorescence probe to ct-DNA. Under the optimum reaction conditions, the linear range was 0.11 × 10^ -5 -0.55 × 10^ -5 mol.L-1, 0. 55 × 10 ^-3 -7.5× 10 ^-5 mol.L-1 with the detection limit of 5.85 × 10 ^-7 mol.L-1.
出处 《稀有金属》 EI CAS CSCD 北大核心 2013年第1期97-103,共7页 Chinese Journal of Rare Metals
基金 国家自然科学基金资助项目(21261018) 教育部科学基金重点项目(208195)资助
关键词 手性 Eu(Ⅲ)配合物 ct—DNA 荧光探针 chiral Eu ( Ⅲ ) complexes ct-DNA fluorescence probe
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  • 1何其庄,杨小飞,钱秀萍,余锡宾,王则民.稀土间氨基苯甲酸8-羟基喹啉三元配合物的合成、表征及抑菌作用研究[J].中国稀土学报,2002,20(z3):1-5. 被引量:23
  • 2何其庄,马树芝,许东芳.稀土酰基吡唑啉酮邻菲咯啉配合物的合成、表征及其生物活性[J].无机化学学报,2007,23(10):1723-1728. 被引量:41
  • 3AurélieClaraz,SylvainOudeyer,VincentLevacher.Chiralquaternaryammoniumaryloxide/N,O-bis(trimethylsilyl)acetamidecombinationasefficientorganocatalyticsystemforthedirectvinylogousaldolreactionof(5H)-furan-2-onederivatives[J].AdvSynthCatal,2013,355:841-846.
  • 4EijiYamamoto,DaichiGokuden,AyanoNagai,etal.Hy-drolyticenantioselectiveprotonationofcyclicdienylestersandaβ-diketonewithchiralphase-transfercatalysts[J].OrgLett,2012,14(24):6178-6181.
  • 5SaraKobbelgaard,MarcoBella,KarlAnkerJrgensen.Im-provedasymmetricSNArreactionof-dicarbonylcom-poundscatalyzedbyquaternaryammonium saltsderivedfromcinchonaalkaloids[J].JOrgChem,2006,71:4980-4987.
  • 6KoheiMatsuzaki,TatsuyaFurukawa,NorioShibata,etal.Highly enantioselective monofluoromethylation of C2-arylindolesusingFBSMunderchiralphase-transfercataly-sis[J].OrgLett,2013,15(13):3282-3285.
  • 7邱凤仙,徐红良,笪祖林,杨冬亚.稀土钕-丙烯酸-草酸配合物的合成、表征及荧光性能(英文)[J].发光学报,2007,28(6):930-934. 被引量:2
  • 8Calherine D S, Lito A, Lykourgos I, Elias S, Dimitris P K. Synthesis and fluorescence properties of rare earth complex with a new diamidel ligand [J]. J. lnorg. Bio- chem., 2002, 89: 89.
  • 9Gear W J. The use of conductivity measurements in or- ganic solvents for the characterization of coordination compounds [ J ]. Coord. Chem. Rev. , 1971, 7 (1) : 81.
  • 10Arivind M, Sageed K. Studies on bis ( p-dimethy lami- nobezy lidene ) benzidine complexes of trivalent lantha- nides [J]. Indian. J. Chem. , 1986, 25A(6) : 589.

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