基于三聚硫氰酸配体的六核镍配合物的合成, 晶体结构和荧光性能分析

陈静 谢吉民 夏昌坤 朱禹 陈佳

引用本文: 陈静, 谢吉民, 夏昌坤, 朱禹, 陈佳. 基于三聚硫氰酸配体的六核镍配合物的合成, 晶体结构和荧光性能分析[J]. 无机化学学报, 2013, 29(11): 2433-2437. doi: 10.3969/j.issn.1001-4861.2013.00.339 shu
Citation:  CHEN Jing, XIE Ji-Min, XIA Chang-Kun, ZHU Yu, CHEN Jia. Synthesis, Characterization and Photoluminescent Property of a Hexanuclear Nickel(Ⅱ) Complex with Trithiocyanuric Acid[J]. Chinese Journal of Inorganic Chemistry, 2013, 29(11): 2433-2437. doi: 10.3969/j.issn.1001-4861.2013.00.339 shu

基于三聚硫氰酸配体的六核镍配合物的合成, 晶体结构和荧光性能分析

  • 基金项目:

    国家自然科学基金(No.21171075/B010303) (No.21171075/B010303)

    教育部博士点基金(No.20093227110009) (No.20093227110009)

    江苏省自然科学基金(No.BK2010166)资助项目。 (No.BK2010166)

摘要: 用缓慢挥发法合成了一个六核Ni(Ⅱ)的配位聚合物[Ni6(H2O)6(HTMT)6]·3(C2H5)3N·7H2O(1)(H3TMT=三聚硫氰酸),并用红外、元素分析及单晶衍射进行表征。该配合物属于三方晶系,R3c空间群,晶胞参数为a=b=1.8697(3)nm,c=3.9825(8)nm,γ=120°。晶胞体积V=12.057(4)nm3,Dc=1.596gcm-3,Z=6,μ=1.91mm-1,F(000)=6095,R=0.047,wR=0.151。X单晶衍射表明,6个Ni(Ⅱ)与6个HTMT2-和6个水分子形成一个六核的构筑单元,这个六核构筑单元又通过氢键作用形成三维结构。同时在室温条件下测定了该配合物的荧光性能。

English

  • 
    1. [1] Wang Y L, Zhang N, Liu Q Y, et al. Cryst. Growth Des., 2011,11:130-138[1] Wang Y L, Zhang N, Liu Q Y, et al. Cryst. Growth Des., 2011,11:130-138

    2. [2] Cao M L, Wu J J, Liang J J, et al. Cryst. Growth Des., 2010,10:4934-4942[2] Cao M L, Wu J J, Liang J J, et al. Cryst. Growth Des., 2010,10:4934-4942

    3. [3] Zigler L M, Wang J, Brewer K B. Inorg. Chem., 2008,47: 11342-11350[3] Zigler L M, Wang J, Brewer K B. Inorg. Chem., 2008,47: 11342-11350

    4. [4] Knoll L M, Arachchige S M, Wang G B. Inorg. Chem., 2011, 50:8850-8860[4] Knoll L M, Arachchige S M, Wang G B. Inorg. Chem., 2011, 50:8850-8860

    5. [5] Henke K R, Robertson D, Krepps M K. Water Res., 2000, 34:3005-3013[5] Henke K R, Robertson D, Krepps M K. Water Res., 2000, 34:3005-3013

    6. [6] Matlock M M, Henke K R, Atwood D A. Water Res., 2001,35:3649-3655[6] Matlock M M, Henke K R, Atwood D A. Water Res., 2001,35:3649-3655

    7. [7] Cecconi F, Ghilardi C A, Midollini S. J. Organomet. Chem., 2002,645:101-104[7] Cecconi F, Ghilardi C A, Midollini S. J. Organomet. Chem., 2002,645:101-104

    8. [8] Haiduc I, Mahon M F, Molloy K C. J. Organomet. Chem., 2001,627:6-12[8] Haiduc I, Mahon M F, Molloy K C. J. Organomet. Chem., 2001,627:6-12

    9. [9] Hunks W J, Jennings M C, Puddephatt R. J. Inorg. Chem., 1999,38:5930-5931[9] Hunks W J, Jennings M C, Puddephatt R. J. Inorg. Chem., 1999,38:5930-5931

    10. [10]Henke K, Atwood D A. Inorg. Chem., 1998,37:224-227[10]Henke K, Atwood D A. Inorg. Chem., 1998,37:224-227

    11. [11]Tzeng B C, Che C M, Peng S M. Chem. Commun., 1997,34: 1771-1772[11]Tzeng B C, Che C M, Peng S M. Chem. Commun., 1997,34: 1771-1772

    12. [12]Chan C K, Cheung K K, Che C M. Chem. Commun., 1996, 34:227-228[12]Chan C K, Cheung K K, Che C M. Chem. Commun., 1996, 34:227-228

    13. [13]Ainscough E W, Brodie A M, Coll R K. Inorg. Chem. Acta, 1993,214:21-22[13]Ainscough E W, Brodie A M, Coll R K. Inorg. Chem. Acta, 1993,214:21-22

    14. [14]Kopel P, Trávnícěk Z, Kvítek L. Polyhedron., 1999,18: 1779-1784[14]Kopel P, Trávnícěk Z, Kvítek L. Polyhedron., 1999,18: 1779-1784

    15. [15]Yamanari K, Kushi Y, Yamamoto M, et al. J. Chem. Soc. Dalton Trans., 1993,24:3715-3721[15]Yamanari K, Kushi Y, Yamamoto M, et al. J. Chem. Soc. Dalton Trans., 1993,24:3715-3721

    16. [16]Clegg W, Davies J E, Elsegood M R J, et al. Inorg. Chem. Commun., 1998,1:58-60[16]Clegg W, Davies J E, Elsegood M R J, et al. Inorg. Chem. Commun., 1998,1:58-60

    17. [17]Corbin D R, Francesconi L C, Hendrickson D N, et al. Inorg. Chem., 1979,18:3069-3074[17]Corbin D R, Francesconi L C, Hendrickson D N, et al. Inorg. Chem., 1979,18:3069-3074

    18. [18]Ainscough E W, Brodie A M, Coll R K, et al. Inorg. Chem. Acta, 1993,214:21-22[18]Ainscough E W, Brodie A M, Coll R K, et al. Inorg. Chem. Acta, 1993,214:21-22

    19. [19]Kar S, Miller T A, Chakraborty S, et al. Dalton Trans., 2003, 12:2591-2596[19]Kar S, Miller T A, Chakraborty S, et al. Dalton Trans., 2003, 12:2591-2596

    20. [20]Kar S, Pradhan B, Sinha R K, et al. J. Chem. Soc., Dalton Trans., 2004,11:1752-1760[20]Kar S, Pradhan B, Sinha R K, et al. J. Chem. Soc., Dalton Trans., 2004,11:1752-1760

    21. [21]Werner H, Steinmetz M, Peters K, et al. Eur. J. Inorg. Chem., 1998,11:1605-1617[21]Werner H, Steinmetz M, Peters K, et al. Eur. J. Inorg. Chem., 1998,11:1605-1617

    22. [22]Fujihara T, Obora Y, Tokunaga M, et al. J. Chem. Soc., Dalton Trans., 2007,16:1567-1569[22]Fujihara T, Obora Y, Tokunaga M, et al. J. Chem. Soc., Dalton Trans., 2007,16:1567-1569

    23. [23]Sheldrick G M. SHELXTL 97, Program for the Refinement of Crystal Structure. University of Gottingen, Germany, 1997.[23]Sheldrick G M. SHELXTL 97, Program for the Refinement of Crystal Structure. University of Gottingen, Germany, 1997.

    24. [24]Liao D M, Luo Y B, Yu P. Appl. Organometal. Chem., 2006,20:246-253[24]Liao D M, Luo Y B, Yu P. Appl. Organometal. Chem., 2006,20:246-253

    25. [25]Kopel P, Trávnícěk Z, Panchá rtková, R. J. Coord. Chem., 1998,44:205-209[25]Kopel P, Trávnícěk Z, Panchá rtková, R. J. Coord. Chem., 1998,44:205-209

    26. [26]Kopel P, Trávnícěk Z, Panchá rtková R. Transition Met. Chem., 1999,24:239-243[26]Kopel P, Trávnícěk Z, Panchá rtková R. Transition Met. Chem., 1999,24:239-243

    27. [27]Li S L, Lan Y Q, Ma J K. Cryst. Growth Des., 2008,8:675-684[27]Li S L, Lan Y Q, Ma J K. Cryst. Growth Des., 2008,8:675-684

    28. [28]Shi X, Zhu G S, Fang Q R. Eur. J. Inorg. Chem., 2004,1: 185-191[28]Shi X, Zhu G S, Fang Q R. Eur. J. Inorg. Chem., 2004,1: 185-191

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  • 收稿日期:  2013-02-16
  • 网络出版日期:  2013-03-18
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