基于对叔丁基杯[8]芳烃的3d-5f核簇化合物(MxThy, M=Co、Ni、Zn)的合成、结构与磁性研究

杜尚超 ,  谭华桥 ,  毕研峰 ,  于洋 ,  廖伍平

引用本文: 杜尚超, 谭华桥, 毕研峰, 于洋, 廖伍平. 基于对叔丁基杯[8]芳烃的3d-5f核簇化合物(MxThy, M=Co、Ni、Zn)的合成、结构与磁性研究[J]. 无机化学学报, 2014, 30(4): 749-756. doi: 10.11862/CJIC.2014.112 shu
Citation:  DU Shang-Chao, TAN Hua-Qiao, BI Yan-Feng, YU Yang, LIAO Wu-Ping. Three 3d-5f Compounds (MxThy, M=Co, Ni, Zn) Based on p-tert-Butylcalix[8]arene:Syntheses, Structures and Magnetic Property[J]. Chinese Journal of Inorganic Chemistry, 2014, 30(4): 749-756. doi: 10.11862/CJIC.2014.112 shu

基于对叔丁基杯[8]芳烃的3d-5f核簇化合物(MxThy, M=Co、Ni、Zn)的合成、结构与磁性研究

    通讯作者: 廖伍平 wpliao@ciac.jl.cn
  • 基金项目:

    国家自然科学基金(21221061,51222404,51074148,91026024) (21221061,51222404,51074148,91026024)

    973项目(2012CBA01206)资助项目。 (2012CBA01206)

摘要: 本文以对叔丁基杯[8]芳烃(H8C8A)为配体,在溶剂热条件下制得了3个3d-5f化合物,[Co2Th4(HC8A)2O2(OH)2(DMF)6](1)、[Ni2Th5(H2C8A)(C8A)O4(OH)2(DMF)5(CH3OH)2](2)、[Zn2Th6(HC8A)(C8A)O5(CH3O)(C3H6NO2)2(DMF)5(CH3OH)](3)(其中H8C8A=对叔丁基杯[8]芳烃,DMF=N,N-二甲基甲酰胺)。X-射线单晶测试表明,这3个化合物均为2个以尾对尾方式排列的杯[8]芳烃分子中间夹1个3d-5f核簇的三明治型结构。杯[8]芳烃均表现为双锥式构型,且每个锥式空腔下缘结合1个钍离子,双锥的连接处及2个杯芳烃分子之间由过渡金属离子或钍离子连接。不同过渡金属离子不同的配位环境导致3种不同核簇的形成。化合物1的磁性研究表明,该化合物在低温下表现出弱铁磁性相互作用。

English

  • 
    1. [1] ZHANG Jia-Hua(张家骅), BAO Bo-Rong(包伯荣), XIA Yuan-Xian(夏源贤). Nucl. Technol. (核技术), 1988, 11(10): 27-33[1] ZHANG Jia-Hua(张家骅), BAO Bo-Rong(包伯荣), XIA Yuan-Xian(夏源贤). Nucl. Technol. (核技术), 1988, 11(10): 27-33

    2. [2] SHEN Chao-Hong(沈朝洪), BAO Ya-Zhi(包亚之), BAO Bo-Rong(包伯荣), et al. J. Nucl. Radiochem. (核化学与放射化 学), 1992, 14(2):94-100[2] SHEN Chao-Hong(沈朝洪), BAO Ya-Zhi(包亚之), BAO Bo-Rong(包伯荣), et al. J. Nucl. Radiochem. (核化学与放射化 学), 1992, 14(2):94-100

    3. [3] ZHANG Li-Qing(张丽清), WANG Zhi-Chang(王之昌), WANG Xiao-Huan(王小欢), et al. J. Nucl. Radiochem. (核化学与放射化学), 2006, 28(1):61-64[3] ZHANG Li-Qing(张丽清), WANG Zhi-Chang(王之昌), WANG Xiao-Huan(王小欢), et al. J. Nucl. Radiochem. (核化学与放射化学), 2006, 28(1):61-64

    4. [4] Borgne T L, Rivière E, Marrot J, et al. Angew. Chem. Int. Ed., 2000, 39:1647-1649[4] Borgne T L, Rivière E, Marrot J, et al. Angew. Chem. Int. Ed., 2000, 39:1647-1649

    5. [5] Maynard B A, Sykora R E, Maguec J T, et al. Chem. Commun., 2010, 46:4944-4946[5] Maynard B A, Sykora R E, Maguec J T, et al. Chem. Commun., 2010, 46:4944-4946

    6. [6] Vaughn A E, Bassil D B, Barnes C L, et al. J. Am. Chem. Soc., 2006, 128:10656-10657[6] Vaughn A E, Bassil D B, Barnes C L, et al. J. Am. Chem. Soc., 2006, 128:10656-10657

    7. [7] Mishra A, Abboud K A, Christou G. Inorg. Chem., 2006, 45: 2364-2366[7] Mishra A, Abboud K A, Christou G. Inorg. Chem., 2006, 45: 2364-2366

    8. [8] YAN Bing(闫冰), ZHANG Hong-Jie(张洪杰), NI Jia-Zan (倪嘉缵). Chem. Res. Appl. (化学研究与应用), 1998, 10(2): 111-117[8] YAN Bing(闫冰), ZHANG Hong-Jie(张洪杰), NI Jia-Zan (倪嘉缵). Chem. Res. Appl. (化学研究与应用), 1998, 10(2): 111-117

    9. [9] Harrowfield J, Koutsantonis G. Calixarenes in the Nanoworld. Dordrecht: Springer, 2007:197[9] Harrowfield J, Koutsantonis G. Calixarenes in the Nanoworld. Dordrecht: Springer, 2007:197

    10. [10] Kajiwara T, Iki N, Yamashita M. Coord. Chem. Rev., 2007, 251:1734-1746[10] Kajiwara T, Iki N, Yamashita M. Coord. Chem. Rev., 2007, 251:1734-1746

    11. [11] Bi Y F, Li Y L, Liao W P, et al. Inorg. Chem., 2008, 47: 9733-9735[11] Bi Y F, Li Y L, Liao W P, et al. Inorg. Chem., 2008, 47: 9733-9735

    12. [12] Bi Y F, Wang X T, Wang B W, et al. Dalton Trans., 2009, 2250-2254[12] Bi Y F, Wang X T, Wang B W, et al. Dalton Trans., 2009, 2250-2254

    13. [13] Karotsis G, Evangelisti M, Dalgarno S J, et al. Angew. Chem. Int. Ed., 2009, 48:9928-9931[13] Karotsis G, Evangelisti M, Dalgarno S J, et al. Angew. Chem. Int. Ed., 2009, 48:9928-9931

    14. [14] Karotsis G, Kennedy S, Teat S J, et al. J. Am. Chem. Soc., 2010, 132:12983-12990[14] Karotsis G, Kennedy S, Teat S J, et al. J. Am. Chem. Soc., 2010, 132:12983-12990

    15. [15] Sanz S, Ferreira K, McIntosh R D, et al. Chem. Commun., 2011, 47:9042-9044[15] Sanz S, Ferreira K, McIntosh R D, et al. Chem. Commun., 2011, 47:9042-9044

    16. [16] Xiong K C, Wang X Y, Jiang F L, et al. Chem. Commun., 2012, 48:7456-7458[16] Xiong K C, Wang X Y, Jiang F L, et al. Chem. Commun., 2012, 48:7456-7458

    17. [17] Su K Z, Jiang F L, Qian J J, et al. Inorg. Chem., 2013, 52: 3780-3786[17] Su K Z, Jiang F L, Qian J J, et al. Inorg. Chem., 2013, 52: 3780-3786

    18. [18] Bergougnant R D, Robin A Y, Fromm K M. Tetrahedron, 2007, 63:10751-10757[18] Bergougnant R D, Robin A Y, Fromm K M. Tetrahedron, 2007, 63:10751-10757

    19. [19] Redshaw C. Coord. Chem. Rev., 2003, 244:45-70[19] Redshaw C. Coord. Chem. Rev., 2003, 244:45-70

    20. [20] DU Shang-Chao(杜尚超), BI Yan-Feng(毕研峰), YU Yang (于洋), et al. Sci. Sin.: Chim.(中国科学: 化学), 2012, 42(9): 1356-1363[20] DU Shang-Chao(杜尚超), BI Yan-Feng(毕研峰), YU Yang (于洋), et al. Sci. Sin.: Chim.(中国科学: 化学), 2012, 42(9): 1356-1363

    21. [21] Gutsche C D, Dhawan B, No K H, et al. J. Am. Chem. Soc., 1981, 103:3782-3792[21] Gutsche C D, Dhawan B, No K H, et al. J. Am. Chem. Soc., 1981, 103:3782-3792

    22. [22] Sheldrick G M. Acta Crystallogr., Sect. A, 2008, 64:112-122[22] Sheldrick G M. Acta Crystallogr., Sect. A, 2008, 64:112-122

    23. [23] Spek A L. J. Appl. Crystallogr., 2003, 36:7-13[23] Spek A L. J. Appl. Crystallogr., 2003, 36:7-13

    24. [24] Harrowfield J M, Ogden M I, White A H. J. Chem. Soc. Dalton Trans., 1991, 2625-2632[24] Harrowfield J M, Ogden M I, White A H. J. Chem. Soc. Dalton Trans., 1991, 2625-2632

    25. [25] Brown I D, Altermatt D. Acta Crystallogr., Sect. B, 1985, 41:244-247[25] Brown I D, Altermatt D. Acta Crystallogr., Sect. B, 1985, 41:244-247

    26. [26] Liu W T, Thorp H H. Inorg. Chem., 1993, 32:4102-4105[26] Liu W T, Thorp H H. Inorg. Chem., 1993, 32:4102-4105

    27. [27] Ugozzoli F, Andreetti G D. J. Inclusion Phenom. Mol. Recognit. Chem., 1992, 13, 337-348[27] Ugozzoli F, Andreetti G D. J. Inclusion Phenom. Mol. Recognit. Chem., 1992, 13, 337-348

    28. [28] Yu J Y, Schreiner S, Vaska L. Inorg. Chim. Acta, 1990, 170: 145-147[28] Yu J Y, Schreiner S, Vaska L. Inorg. Chim. Acta, 1990, 170: 145-147

    29. [29] Langley S, Helliwell M, Sessoli R, et al. Inorg. Chem., 2008, 47:497-507[29] Langley S, Helliwell M, Sessoli R, et al. Inorg. Chem., 2008, 47:497-507

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  • 收稿日期:  2013-07-13
  • 网络出版日期:  2013-11-20
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