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-  2015 


DOI: 10.3866/PKU.WHXB201510084

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Abstract:

设计并制备三种具不同官能团的铱[III]邻菲啰啉配合物: [Ir(ppy)2phen-Br]Cl, [Ir(ppy)2phen-COOH]Cl, [Ir(ppy)2phen-Si]Cl,以及对比参照物[Ir(ppy)2phen-NH2]Cl.其中, ppy为2-苯基吡啶, phen-Br为2-溴-2甲基-N-(1, 10-菲啰啉-5-基)丙酰胺, phen-COOH为4-[(1, 10-菲啰啉-5-基)氨基]-4-酰基丁烯酸, phen-Si为5-[N, N-二-3-(三乙氧硅)基]酰亚胺-1, 10-菲啰啉, phen-NH2为5-氨基-邻菲啰啉,并采用核磁共振(NMR)、质谱(MS)、紫外-可见(UV-Vis)吸收光谱、荧光(PL)光谱法和循环伏安法(CV)等对上述配合物进行了分析和表征.光物理性能研究结果表明:这些配合物在蓝-紫色可见光区域有较强吸收,可发射出明亮的黄色到橙红色荧光,量子效率达到12%以上.相比较于参照物[Ir(ppy)2phen-NH2]Cl (5.78 μs),三种新型配合物在量子效率未明显降低甚至提高的前提下,荧光寿命有了显著的提高(9.18-12.00 μs).其中, [Ir(ppy)2phen-Br]Cl (1)不但有最高的荧光量子产率(32%)和最长的荧光寿命(12.00 μs),而且也具有最好的氧传感性能, I0/I (无氧与纯氧条件下的荧光强度比值)可达到10.91.这使得[Ir(ppy)2phen-Br]Cl有望成为接枝型,较高性能的光学氧传感器的候选氧敏指示剂.除此之外,还通过含时密度泛函理论(TD-DFT)计算对配合物光电性能进行补充说明,理论计算表明:这些配合物是以铱为中心的近似八面体结构,理论计算结果与实际实验数据相一致.
A series of luminescent cyclometalated Ir(III) complexes functionalized with amide derivatives were prepared and compared with [Ir(ppy)2phen-NH2]Cl. The complexes were [Ir(ppy)2phen-Br]Cl, [Ir(ppy)2phen-COOH]Cl, and [Ir(ppy)2phen-Si]Cl, where ppy is 2-phenylpyridine, phen-NH2 is 5-amino-[1, 10]-phenanthroline, phen-Br is 2-bromo-2-methyl-N-(1, 10-phenanthrolin-5-yl)propanamide, phen-COOH is 4-[(1, 10-phenanthrolin-5-yl)amino]-4-oxobut-2-enoic acid, and phen-Si is 5-[N, N-bis-3-(triethoxysilyl) propyl]ureyl-1, 10-phenanthroline. They were characterized using nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), ultraviolet-visible (UV-Vis) absorption spectroscopy, photoluminescence (PL) spectroscopy, and cyclic voltammetry (CV). The three novel complexes have intense absorptions in the blue-purple region. The complexes show bright yellow to orange PL emissions under UV irradiation, and the quantum yields (Φ) of these complexes are higher than 12%. The excited-state lifetimes of the novel complexes are 9.18-12.00 μs, much longer than that of [Ir(ppy)2phen-NH2]Cl (5.78 μs). With both the highest quantum yield (32%) and longest lifetime (12.00 μs), [Ir(ppy)2phen-Br]Cl also shows the best oxygen-sensing properties and the largest I0/I factor, 10.91 (I0: the PL intensity of the complex in the absence of O2, I: the PL intensity of the complex under pure oxygen). These results suggest that [Ir(ppy)2phen-Br]Cl may be a promising candidate for use in oxygen sensors based on covalent grafting. Time-dependent density functional theory (TD-DFT) calculations were used to supplement the photoelectric property studies. Theoretical calculations indicate that all the mononuclear complexes have approximately octahedral structures with Ir(III) as the coordination center. The computational results agree well with the

References

[1]  5 Lupo F. ; Fragala M. E. ; Gupta T. ; Mamo A. ; Aureliano A. ; Bettinelli M. ; Speghini A. ; Gulino A. J. Phys. Chem. C 2010, 114, 13459. doi: 10.1021/Jp1028917
[2]  岳岩; 许慧侠; 郝玉英; 解晓东; 屈丽桃; 王华; 许并社. 物理化学学报, 2012, 28, 1593. doi: 10.3866/PKU.WHXB201204181
[3]  23 Ren J. K. ; Xu H. X. ; Qu L. T. ; Hao Y. Y. ; Wang H. ; Xu B. S. Acta Phys. -Chim. Sin 2013, 29, 1115. doi: 10.3866/PKU.WHXB201302253
[4]  26 Ohsawa Y. ; Sprouse S. ; King K. A. ; Dearmond M. K. ; Hanck K. W. ; Watts R. J. J. Phys. Chem 1987, 91, 1047. doi: 10.1021/J100289a009
[5]  27 Lowry M. S. ; Hudson W. R. ; Pascal R. A. ; Bernhard S. J. Am. Chem. Soc 2004, 126, 14129. doi: 10.1021/Ja047156+
[6]  30 Di Marco G. ; Lanza M. ; Mamo A. ; Stefio I. ; Di Pietro C. ; Romeo G. ; Campagna S. Anal. Chem 1998, 70, 5019. doi: 10.1021/ac980234p
[7]  32 Lu X. ; Manners I. ; Winnik M. A. Macromolecules 2001, 34, 1917. doi: 10.1021/Ma001454j
[8]  33 Hocker G. B. Appl. Opt 1979, 18, 1445. doi: 10.1364/Ao.18.001445
[9]  34 Klimant I. ; Wolfbeis O. S. Anal. Chem 1995, 67, 3160. doi: 10.1021/Ac00114a010
[10]  40 Li H. R. ; Lin J. ; Zhang H. J. ; Li H. C. ; Fu L. S. ; Meng Q. G. Chem. Commun 2001, 1212 doi: 10.1039/b102160p
[11]  48 Lo K. K. W. ; Ng D. C. M. ; Chung C. K. Organometallics 2001, 20, 4999. doi: 10.1021/Om010652b
[12]  49 Li H. R. ; Lin J. ; Zhang H. J. ; Fu L. S. ; Meng Q. G. ; Wang S. B. Chem. Mater 2002, 14, 3651. doi: 10.1021/Cm0116830
[13]  50 Okutsu T. ; Ishihara A. ; Kounose N. ; Suzuki H. H. T. ; Ichimura T. ; Hiratsuka H. J. Photochem. Photobiol. A 2007, 186, 229. doi: 10.1016/j.jphotochem.2006.08.019
[14]  51 Sun Y. ; Liang X. H. ; Zhao Y. Y. ; Fan J. Spectrochim. Acta A 2013, 102, 194. doi: 10.1016/j.saa.2012.10.013
[15]  54 Tang L. ; Qi Z. J. ; Hong M. X. ; Li N. ; Wei S. ; Yang F. ; Ji X. ; Hu A. J. Acta Chim. Sin 2012, 70, 1081. doi: 10.6023/A1112121
[16]  55 Wang J. X. ; Xia H. Y. ; Liu W. Q. ; Zhao F. ; Wang Y. B. Inorg. Chim. Acta 2013, 394, 92. doi: 10.1016/j.ica.2012.07.032
[17]  1 Zelelow B. ; Khalil G. E. ; Phelan G. ; Carlson B. ; Gouterman M. ; Callis J. B. ; Dalton L. R. Sensor Actuat. B-Chem 2003, 96, 304. doi: 10.1016/S0925-4005(03)00547-1
[18]  3 Borisov S. M. ; Wolfbeis O. S. Anal. Chem 2006, 78, 5094. doi: 10.1021/Ac060311d
[19]  9 Zhang S. J. ; Hosaka M. ; Yoshihara T. ; Negishi K. ; Iida Y. ; Tobita S. ; Takeuchi T. Cancer Res 2010, 70, 4490. doi: 10.1158/0008-5472.Can-09-3948
[20]  11 Dixon I. M. ; Collin J. P. ; Sauvage J. P. ; Flamigni L. ; Encinas S. ; Barigelletti F. Chem. Soc. Rev 2000, 29, 385. doi: 10.1039/B000704h
[21]  28 Medina-Castillo A. L. ; Fernandez-Sanchez J. F. ; Klein C. ; Nazeeruddin M. K. ; Segura-Carretero A. ; Fernandez-Gutierrez A. ; Gr? tzel M. ; Spichiger-Keller U. E. Analyst 2007, 132, 929. doi: 10.1039/b702628e
[22]  35 Wang H. Y. ; Xu G. B. ; Dong S. J. Analyst 2001, 126, 1095. doi: 10.1039/b100376n
[23]  36 Hubner J. P. ; Carroll B. F. ; Schanze K. S. ; Ji H. F. Exp. Fluids 2000, 28, 21. doi: 10.1007/s003480050003
[24]  38 Bedlek-Anslow J. M. ; Hubner J. P. ; Carroll B. F. ; Schanze K. S. Langmuir 2000, 16, 9137. doi: 10.1021/La0011679
[25]  39 Lu X. ; Winnik M. A. Chem. Mater 2001, 13, 3449. doi: 10.1021/Cm011029k
[26]  46 Reetz M. T. ; Rentzsch M. ; Pletsch A. ; Taglieber A. ; Hollmann F. ; Mondiere R. J. G. ; Dickmann N. ; Hocker B. ; Cerrone S. ; Haeger M. C. ; Sterner R. ChemBioChem 2008, 9, 552. doi: 10.1002/cbic.200700413
[27]  52 Rodríguez-Romero J. ; Aparicio-Ixta L. ; Rodríguez M. ; Ramos-Ortíz G. ; Maldonado J. L. ; Jiménez-Sánchez A. ; Farfán N. ; Santillan R. Dyes Pigments 2013, 98, 31. doi: 10.1016/j.dyepig.2012.12.029
[28]  唐兰兰; 祁争健; 洪满心; 李楠; 沈伟; 杨帆; 吉昕; 胡爱江. 化学学报, 2012, 70, 1081. doi: 10.6023/A1112121
[29]  56 Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; et al. Gaussian 03, Revision B.05; Gaussian Inc.; Pittsburgh, PA, 2003.
[30]  6 Schroder C. R. ; Polerecky L. ; Klimant I. Anal. Chem 2007, 79, 60. doi: 10.1021/Ac0606047
[31]  7 Borisov S. M. ; Krause C. ; Arain S. ; Wolfbeis O. S. Adv. Mater 2006, 18, 1511. doi: 10.1002/adma.200600120
[32]  8 Lo K. K. W. ; Li S. P. Y. ; Zhang K. Y. ; New J. Chem 2011, 35, 265. doi: 10.1039/C0nj00478b
[33]  10 Williams J. A. Chem. Soc. Rev 2009, 38, 1783. doi: 10.1039/b804434c
[34]  12 Ulbricht C. ; Beyer B. ; Friebe C. ; Winter A. ; Schubert U. S. Adv. Mater 2009, 21, 4418. doi: 10.1002/adma.200803537
[35]  13 Whittle V. L. ; Williams J. A. Dalton Trans 2009, 3929 doi: 10.1039/b821161b
[36]  14 You Y. ; Park S. Y. Dalton Trans 2009, 1267 doi: 10.1039/b812281d
[37]  17 Lo K. K. W. ; Louie M. W. ; Zhang K. Y. Coordin. Chem. Rev 2010, 254, 2603. doi: 10.1016/j.ccr.2010.01.014
[38]  19 Chi Y. ; Chou P. T. Chem. Soc. Rev 2010, 39, 638. doi: 10.1039/b916237b
[39]  20 Yue Y. ; Xu H. X. ; Hao Y. Y. ; Xie X. D. ; Qu L. T. ; Wang H. ; Xu B. S. Acta Phys. -Chim. Sin 2012, 28, 1593. doi: 10.3866/PKU.WHXB201204181
[40]  22 Wang L. X. ; Mei Q. B. ; Yan F. ; Tian B. ; Weng J. N. ; Zhang B. ; Huang W. Acta Phys. -Chim. Sin 2012, 28, 1556. doi: 10.3866/PKU.WHXB201205043
[41]  45 dos Santos C. M. G. ; Gunnlaugsson T. Supramol. Chem 2009, 21, 173. doi: 10.1080/10610270802588285
[42]  2 Borisov S. M. ; Vasylevska A. S. ; Krause C. ; Wolfbeis O. S. Adv. Funct. Mater 2006, 16, 1536. doi: 10.1002/adfm.200500778
[43]  4 Kose M. E. ; Carroll B. F. ; Schanze K. S. Langmuir 2005, 21, 9121. doi: 10.1021/La050997p
[44]  15 Fernandez-Moreira V. ; Thorp-Greenwood F. L. ; Coogan M. P. Chem Commun (Camb) 2010, 46, 186. doi: 10.1039/b917757d
[45]  16 Zhao Q. ; Li F. ; Huang C. Chem. Soc. Rev 2010, 39, 3007. doi: 10.1039/b915340c
[46]  18 Lo K. K. W. Photophysics of Organometallics 2010, 29, 115. doi: 10.1007/3418_2009_3
[47]  21 Wei C. D. ; Ge G. P. ; Li C. Y. ; Lei K. W. ; Liang H. Z. ; Yu G. ; Liu Z. W. Acta Phys. -Chim. Sin 2015, 31, 17. doi: 10.3866/PKU.WHXB201411212
[48]  韦传东; 葛国平; 李春艳; 雷克微; 梁洪泽; 禹钢; 刘志伟. 物理化学学报, 2015, 31, 17. doi: 10.3866/PKU.WHXB201411212
[49]  王玲霞; 梅群波; 颜芳; 田波; 翁洁娜; 张彬; 黄维. 物理化学学报, 2012, 28, 1556. doi: 10.3866/PKU.WHXB201205043
[50]  任静琨; 许慧侠; 屈丽桃; 郝玉英; 王华; 许并社. 物理化学学报, 2013, 29, 1115. doi: 10.3866/PKU.WHXB201302253
[51]  24 DeRosa M. C. ; Mosher P. J. ; Yap G. P. A. ; Focsaneanu K. S. ; Crutchley R. J. ; Evans C. E. B. Inorg. Chem 2003, 42, 4864. doi: 10.1021/Ic026230r
[52]  25 Huynh L. ; Wang Z. U. ; Yang J. ; Stoeva V. ; Lough A. ; Manners I. ; Winnik M. A. Chem. Mater 2005, 17, 4765. doi: 10.1021/cm047794r
[53]  29 Habibagahi A. ; Mebarki Y. ; Sultan Y. ; Yap G. P. ; Crutchley R. J. ACS Appl. Mater. Interfaces 2009, 1, 1785. doi: 10.1021/am900306a
[54]  31 Xu W. Y. ; Ma W. T. ; Li K. Y. ; Hu J. M. ; Shen L. R. ; Li H. Y. ; Cao L. X. Sensor Actuat. B-Chem 2002, 86, 174. doi: 10.1016/s0925-4005(02)00165-x
[55]  37 Tang Y. ; Tehan E. C. ; Tao Z. Y. ; Bright F. V. Anal. Chem 2003, 75, 2407. doi: 10.1021/Ac030087h
[56]  41 Xavier M. P. ; Garcia-Fresnadillo D. ; Moreno-Bondi M. C. ; Orellana G. Anal. Chem 1998, 70, 5184. doi: 10.1021/Ac980722x
[57]  42 Wang Z. ; McWilliams A. R. ; Evans C. E. B. ; Lu X. ; Chung S. ; Winnik M. A. ; Manners I. Adv. Funct. Mater 2002, 12, 415. doi: 10.1002/1616-3028(20020618)12:6/7<415::Aid-Adfm415>3.0.Co;2-Y
[58]  43 Franville A. C. ; Mahiou R. ; Zambon D. ; Cousseins J. C. Solid State Sci 2001, 3, 211. doi: 10.1016/S1293-2558(00)01114-6
[59]  44 Sprouse S. ; King K. A. ; Spellane P. J. ; Watts R. J. J. Am. Chem. Soc 1984, 106, 6647. doi: 10.1021/Ja00334a031
[60]  47 Lee S. J. ; Bae D. R. ; Han W. S. ; Lee S. S. ; Jung J. H. Eur. J. Inorg. Chem 2008, 2008, 1559. doi: 10.1002/ejic.200701073
[61]  53 Malins C. ; Glever H. G. ; MacCraith B. D. ; Fanni S. ; Vos J. G. Anal. Commun 1999, 36, 3. doi: 10.1039/a808731h

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