注册 English

两个4-[(8-羟基-5-喹啉)偶氮]苯磺酸配合物的合成、结构及性质研究

罗亚楠 ,  许宪祝 ,  张潇 ,  于晓洋 ,  曲小姝

downloadPDF
引用本文: 罗亚楠, 许宪祝, 张潇, 于晓洋, 曲小姝. 两个4-[(8-羟基-5-喹啉)偶氮]苯磺酸配合物的合成、结构及性质研究[J]. 无机化学学报, 2013, 29(12): 2655-2665. doi: 10.3969/j.issn.1001-4861.2013.00.389 shu
Citation:  LUO Ya-Nan, XU Xian-Zhu, ZHANG Xiao, YU Xiao-Yang, QU Xiao-Shu. Syntheses, Structures and Properties of Two Coordination Polymers with 4-[(8-Hydroxy-5-quinolinyl)azo]-benzenesulfonic Acid[J]. Chinese Journal of Inorganic Chemistry, 2013, 29(12): 2655-2665. doi: 10.3969/j.issn.1001-4861.2013.00.389 shu

两个4-[(8-羟基-5-喹啉)偶氮]苯磺酸配合物的合成、结构及性质研究

  • 基金项目:

    国家973项目(No.2012CB821700)，NSFC国际合作研究项目(No.21120102034；20831002)，国家自然科学基金(No.51108122) (No.2012CB821700)，NSFC国际合作研究项目(No.21120102034；20831002)，国家自然科学基金(No.51108122)

    吉林省教育厅(No.2013-328)资助项目 (No.2013-328)

摘要: 以4-[(8-羟基-5-喹啉)偶氮]苯磺酸(H2L)为配体，采用溶剂热合成法合成了两个配合物[CuL(en)]·0.5H2O (1)和[CuL2][Cu(en)2]·2H2O (2)(en=乙二胺)，并采用单晶X-射线衍射、红外光谱、元素分析、X-射线粉末衍射和热重分析对其进行表征。化合物1和2通过氢键和π…π相互作用连接形成了三维超分子网格。此外，还研究了两个化合物的荧光性质。

English

  • 

    1. [1] Daniel M C, Astruc D. Chem. Rev., 2004, 104:293-346[1] Daniel M C, Astruc D. Chem. Rev., 2004, 104:293-346

    2. [2] Kitagawa S, Kitaura R, Noro S. Angew. Chem. Int. Ed., 2004, 43:2334-2375[2] Kitagawa S, Kitaura R, Noro S. Angew. Chem. Int. Ed., 2004, 43:2334-2375

    3. [3] Eddaoudi M, Moler D B, Li H L, et al. Acc. Chem. Res., 2001, 34 (4):319-330[3] Eddaoudi M, Moler D B, Li H L, et al. Acc. Chem. Res., 2001, 34 (4):319-330

    4. [4] YANG Ying-Qun (杨颖群), CHEN Man-Sheng (陈满生), CHEN Zhi-Min (陈志敏), et al. Chinese J. Inorg. Chem. (Wuji Huaxue Xuebao), 2011, 27 (9):1847-1851[4] YANG Ying-Qun (杨颖群), CHEN Man-Sheng (陈满生), CHEN Zhi-Min (陈志敏), et al. Chinese J. Inorg. Chem. (Wuji Huaxue Xuebao), 2011, 27 (9):1847-1851

    5. [5] Yaghi O M, O′Keeffe M, Ockwig N W, et al. Nature, 2003, 423:705-714[5] Yaghi O M, O′Keeffe M, Ockwig N W, et al. Nature, 2003, 423:705-714

    6. [6] Tranchemontagne D J, Mendoza-Corté s J L, O′Keeffe M, et al. Chem. Soc. Rev., 2009, 38:1257-1283[6] Tranchemontagne D J, Mendoza-Corté s J L, O′Keeffe M, et al. Chem. Soc. Rev., 2009, 38:1257-1283

    7. [7] Kolotuchin S V, Fenlon E E, Wilson S R, et al. Angew. Chem. Int. Ed., 1995, 34:2654-2657[7] Kolotuchin S V, Fenlon E E, Wilson S R, et al. Angew. Chem. Int. Ed., 1995, 34:2654-2657

    8. [8] Wang X L, Qin C, Wu S X, et al. Angew. Chem. Int. Ed., 2009, 48 (29):5291-5295[8] Wang X L, Qin C, Wu S X, et al. Angew. Chem. Int. Ed., 2009, 48 (29):5291-5295

    9. [9] Dikarev E V, Li B, Chernyshev V V, et al. Chem. Commun., 2005:3274-3276[9] Dikarev E V, Li B, Chernyshev V V, et al. Chem. Commun., 2005:3274-3276

    10. [10] ZHU Dun-Ru (朱敦如), ZHOU Jun (周俊), YANG Jie (杨 捷), et al. J. Nanjing Univ. Tech. (Nanjing Gongye Daxue Xuebao), 2007, 29:103-110[10] ZHU Dun-Ru (朱敦如), ZHOU Jun (周俊), YANG Jie (杨 捷), et al. J. Nanjing Univ. Tech. (Nanjing Gongye Daxue Xuebao), 2007, 29:103-110

    11. [11] XIA Jun (夏军), ZHANG Ming (张明), ZHAO Bin (赵斌), et al. Chinese J. Inorg. Chem. (Wuji Huaxue Xuebao), 2006, 22 (8):1406-1410[11] XIA Jun (夏军), ZHANG Ming (张明), ZHAO Bin (赵斌), et al. Chinese J. Inorg. Chem. (Wuji Huaxue Xuebao), 2006, 22 (8):1406-1410

    12. [12] Larsen R W. J. Am. Chem. Soc., 2008, 130:11246-11247[12] Larsen R W. J. Am. Chem. Soc., 2008, 130:11246-11247

    13. [13] Xu G C, Ding Y J, Okamura T A, et al. CrystEngComm, 2008, 10:1052-1062[13] Xu G C, Ding Y J, Okamura T A, et al. CrystEngComm, 2008, 10:1052-1062

    14. [14] Luo F, Che Y X, Zheng J M. Cryst. Growth Des., 2008, 8: 176-178[14] Luo F, Che Y X, Zheng J M. Cryst. Growth Des., 2008, 8: 176-178

    15. [15] Zeng M H, Wang Q X, Tan Y X, et al. J. Am. Chem. Soc., 2010, 132:2561-2563[15] Zeng M H, Wang Q X, Tan Y X, et al. J. Am. Chem. Soc., 2010, 132:2561-2563

    16. [16] Long J R, Bloch E D, Britt D, et al. J. Am. Chem. Soc., 2010, 132:14382-14384[16] Long J R, Bloch E D, Britt D, et al. J. Am. Chem. Soc., 2010, 132:14382-14384

    17. [17] Katsoulis D E. Chem. Rev., 1998, 98:359-388[17] Katsoulis D E. Chem. Rev., 1998, 98:359-388

    18. [18] MÜ ller A. Serain C. Acc. Chem. Res., 2000, 33:2-10[18] MÜ ller A. Serain C. Acc. Chem. Res., 2000, 33:2-10

    19. [19] Liu W L, Ye L H, Liu X F, et al. CrystEngComm, 2008, 10: 1395-1403[19] Liu W L, Ye L H, Liu X F, et al. CrystEngComm, 2008, 10: 1395-1403

    20. [20] Chen Z F, Xiong R G, Abrahams B F, et al. J. Chem. Soc. Dalton Trans., 2001, 17:2453-2455[20] Chen Z F, Xiong R G, Abrahams B F, et al. J. Chem. Soc. Dalton Trans., 2001, 17:2453-2455

    21. [21] Reineke T M, Eddaoudi M, Moler D B, et al. J. Am. Chem. Soc., 2000, 122:4843-4844[21] Reineke T M, Eddaoudi M, Moler D B, et al. J. Am. Chem. Soc., 2000, 122:4843-4844

    22. [22] Chen Z F, Zhang Z L, Tan Y H, et al. CrystEngComm, 2008, 10:217-231[22] Chen Z F, Zhang Z L, Tan Y H, et al. CrystEngComm, 2008, 10:217-231

    23. [23] Balasubramani K, Thomas P, Bocelli G, et al. J. Coord. Chem., 2005, 58:1689-1694[23] Balasubramani K, Thomas P, Bocelli G, et al. J. Coord. Chem., 2005, 58:1689-1694

    24. [24] Lu Y G, Cheng W, Meng X R, et al. J. Mol. Struct., 2008, 875:183-188[24] Lu Y G, Cheng W, Meng X R, et al. J. Mol. Struct., 2008, 875:183-188

    25. [25] Thomas M P, Murugesan S. J. Coord. Chem., 2006, 59:1167-1172[25] Thomas M P, Murugesan S. J. Coord. Chem., 2006, 59:1167-1172

    26. [26] Camerel F, Barberá J, Otsuki J, et al. Adv. Mater., 2008, 20: 3462-3467[26] Camerel F, Barberá J, Otsuki J, et al. Adv. Mater., 2008, 20: 3462-3467

    27. [27] Park J S, Jeong S, Dho S K, et al. Dyes Pigm., 2010, 87:49-54[27] Park J S, Jeong S, Dho S K, et al. Dyes Pigm., 2010, 87:49-54

    28. [28] AytÜ l S, Zeynel S, Nermin E. Dyes Pigm., 2008, 76 (2):470-476[28] AytÜ l S, Zeynel S, Nermin E. Dyes Pigm., 2008, 76 (2):470-476

    29. [29] Sheldrick G M. SHELXTL V. 5.10. Structure Determination Software Suite, Bruker AXS, Madison, 1998.[29] Sheldrick G M. SHELXTL V. 5.10. Structure Determination Software Suite, Bruker AXS, Madison, 1998.

    30. [30] Dolomanov O V, Bourhis L J, Gildea R J, et al. J. Appl. Cryst., 2009, 42:339-341[30] Dolomanov O V, Bourhis L J, Gildea R J, et al. J. Appl. Cryst., 2009, 42:339-341

    31. [31] Spek A L, Appl J. J. Appl. Crystallogr., 2003, 36:7-13[31] Spek A L, Appl J. J. Appl. Crystallogr., 2003, 36:7-13

    32. [32] Spek A L. PLATON, A Multipurpose Crystallographic Tool, Utrecht University, Netherlands, 2006.[32] Spek A L. PLATON, A Multipurpose Crystallographic Tool, Utrecht University, Netherlands, 2006.

    33. [33] Yuan L, Qin C, Wang X L, et al. Solid State Sci., 2008, 10: 967-975[33] Yuan L, Qin C, Wang X L, et al. Solid State Sci., 2008, 10: 967-975

    34. [34] Yu X Y, Ye L, Zhang X, et al. Dalton Trans., 2010, 39 (44): 10617-10625[34] Yu X Y, Ye L, Zhang X, et al. Dalton Trans., 2010, 39 (44): 10617-10625

    35. [35] Lan A J, Padmanabhan M, Li K H, et al. Inorg. Chim. Acta, 2011, 366:68-75[35] Lan A J, Padmanabhan M, Li K H, et al. Inorg. Chim. Acta, 2011, 366:68-75

  • 加载中
WeChat 扫一扫看文章
计量
  • PDF下载量:  0
  • 文章访问数:  527
  • HTML全文浏览量:  20
文章相关
  • 收稿日期:  2013-02-20
  • 网络出版日期:  2013-06-27
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

/

返回文章

All Rights Reserved by the Chinese Chemical Society   中国化学会 版权所有 京ICP备05002797号

本系统由北京仁和汇智信息技术有限公司开发    技术支持: info@rhhz.net