DOI QR코드

DOI QR Code

Two-Dimensional Nickel Coordination Polymers: Ni(OBC)(bipyen)]·H2O and [Ni(NDC)(bipyen)(H2O)] (NDC = 2,6-Naphthalenedicarboxylate; OBC = 4,4'-Oxybis(benzoate); bipyen = trans-1,2-Bis(4-pyridyl)ethylene)

  • Lee, Yeon-Kyoung (Department of Chemistry (BK21), Sungkyunkwan University) ;
  • Lee, Soon W. (Department of Chemistry (BK21), Sungkyunkwan University)
  • Published : 2003.07.20

Abstract

Hydrothermal reactions of Ni(NO₃)₂· 6H₂O with trans-1,2-bis(4-pyridyl)ethylene (bipyen), in the presence of a linear 2,6-naphthalene dicarboxylic acid (NDCH₂) and a bent 4,4'-oxybis(benzoic acid) (OBCH₂), gave a 2-D coordination polymer [Ni(NDC)(bipyen)(H₂O)] (1) and also a 2-D coordination polymer [Ni(OBC)(bipyen)]· H₂O (2), respectively. A reversible de-coordination and re-coordination of an aqua ligand was observed for polymer 1. Polymer 2 has an undulated 2-D network based on 50-membered rectangular grids, each of which has the dimension of 13.61 × 13.17 Å.

Keywords

References

  1. Breck, D. W. Zeolite Molecular Sieves; John Wilkey & Sons: New York, 1974
  2. Bhatia, S. Zeolite Catalysts: Principles and Applications; CRC Press, Inc.: Boca Raton, 1990.
  3. Batten, S. R.; Robson, R. Angew. Chem., Int. Ed. 1998, 37,1461.
  4. Munakata, M.; Wu, L. P.; Kuroda, S. T. Adv. Inorg.Chem. 1999, 46, 173.
  5. Hagrman, P. J.; Hagrman, D.; Zubieta, J.Angew. Chem., Int. Ed. 1999, 38, 2638. https://doi.org/10.1002/(SICI)1521-3773(19990917)38:18<2638::AID-ANIE2638>3.0.CO;2-4
  6. OKeeffe, M.;Eddaoudi, M.; Li, H.; Yaghi, O. M. J. Solid State Chem. 2000,152, 3. https://doi.org/10.1006/jssc.2000.8723
  7. Eddaoudi, M.; Moler, D. B.; Li, H.; Chen, B.; Reineke,T. M.; OKeeffe, M.; Yaghi, O. M. Acc. Chem. Res. 2001, 34, 319. https://doi.org/10.1021/ar000034b
  8. Zaworotko, M. J.; Moulton, B. Chem. Rev. 2001, 101, 629.
  9. Yaghi, O. M.; Li, H.; Davis, C.; Richardson, D.; Groy, T. L.Acc. Chem. Res. 1998, 31, 474. https://doi.org/10.1021/ar970151f
  10. Mori, W.; Takamizawa, S. J.Solid State Chem. 2000, 152, 120. https://doi.org/10.1006/jssc.2000.8675
  11. Noro, S. I.; Kitaura, R.;Kondo, M.; Kitagawa, S.; Ishii, T.; Matsuzaka, H.; Yamashita, M.J. Am. Chem. Soc. 2002, 124, 2568. https://doi.org/10.1021/ja0113192
  12. Kasai, K.; Aoyagi, M.; Fujita, M. J. Am. Chem. Soc. 2000, 122,2140. https://doi.org/10.1021/ja992553j
  13. Shi, Z.; Zhang, L.; Gao, S.; Yang, G.; Hua, J.; Feng, S.Inorg. Chem. 2000, 39, 1990. https://doi.org/10.1021/ic991355q
  14. Cui, Y.; Ngo, H. L.; Lin, W. Inorg. Chem. 2002, 41, 1033. https://doi.org/10.1021/ic015627c
  15. Bourne, S. A.; Lu, J.; Moulton, B.; Zaworotko, M. J. Chem.Commun. 2001, 861.
  16. Ko, J. W.; Min, K. S.; Pack Suh, M. H.Inorg. Chem. 2002, 41, 2151. https://doi.org/10.1021/ic011281u
  17. Li, H.; Eddaudi, M.; Groy, T. L.; Yaghi, O. M. J. Am. Chem.Soc. 1998, 120, 8571. https://doi.org/10.1021/ja981669x
  18. Pan, L.; Woodlock, E. B.; Wang, X.Inorg. Chem. 2000, 39, 4174. https://doi.org/10.1021/ic000209d
  19. Pan, L.; Zheng, N.; Wu, Y.; Han,S.; Yang, R.; Huang, X.; Li, J. Ionrg. Chem. 2001, 40, 828. https://doi.org/10.1021/ic0007254
  20. Seki, K.; Mori, W. J. Phys. Chem. B 2002, 106, 1380. https://doi.org/10.1021/jp0130416
  21. Lu, J. Y.; Cabrera, B. R.; Wang, R. J.; Li, J. Inorg. Chem. 1999,38, 4608. https://doi.org/10.1021/ic990536p
  22. Lu, J.; Yu, C.; Niu, T.; Paliwala, T.; Crisci, G.;Somosa, F.; Jacobson, A. J. Inorg. Chem. 1998, 37, 4637. https://doi.org/10.1021/ic971614g
  23. Fujita, M.; Kwon, Y. T.; Washizu, S.; Ogura, K. J. Am. Chem. Soc.1994, 116, 1151. https://doi.org/10.1021/ja00082a055
  24. Knaust, J. M.; Keller, S. W. Inorg. Chem.2002, 41, 5650. https://doi.org/10.1021/ic025836c
  25. Wu, C. D.; Lu, C. Z.; Lu, S. F.; Zhuang, H. H.; Huang, J. S.Inorg. Chem. Commun. 2002, 5, 171. https://doi.org/10.1016/S1387-7003(02)00325-8
  26. Tao, J.; Zang, Y.; Tong,M.-L.: Chen, X.-M.; Yuen, T.; Lin, C. L.; Huang, X.; Li, J. Chem.Commun. 2002, 1342.
  27. Shi, Z.; Feng, S.; Sun, Y.; Hau, J. Inorg.Chem. 2001, 40, 5312. https://doi.org/10.1021/ic015518y
  28. Min, D.; Yoon, S. S.; Lee, C. Y.; Suh, M.; Hwang, Y. J.; Han,W. S.; Lee, S. W. Bull. Korean Chem. Soc. 2001, 22, 531.
  29. Min,D.; Yoon, S. S., Lee, J. H.; Suh, M.; Lee, S. W. Inorg. Chem.Commun. 2001, 4, 297. https://doi.org/10.1016/S1387-7003(01)00197-6
  30. Min, D.; Yoon, S. S.; Lee, C. Y.; Han,W. S.; Lee, S. W. Bull. Korean Chem. Soc. 2001, 22, 1041.
  31. Min, D.; Yoon, S. S.; Jung, D.-Y.; Lee, C. Y.; Kim, Y.; Han, W. S.;Lee, S. W. Inorg. Chim. Acta 2001, 324, 293. https://doi.org/10.1016/S0020-1693(01)00621-1
  32. Huh, H. S.; Min,D. W.; Lee, Y. K.; Lee, S. W. Bull. Korean Chem. Soc. 2002, 23,619. https://doi.org/10.5012/bkcs.2002.23.4.619
  33. Min, D.; Yoon, S. S.; Lee, S. W. Inorg. Chem. Commun.2002, 5, 143. https://doi.org/10.1016/S1387-7003(01)00366-5
  34. Min, D.; Lee, S. W. Inorg. Chem. Commun.2002, 5, 978. https://doi.org/10.1016/S1387-7003(02)00630-5
  35. Min, D.; Lee, S. W. Bull. Korean Chem. Soc.2002, 23, 948. https://doi.org/10.1007/s11814-006-0013-3
  36. Baeg, J. Y.; Lee, S. W. Inorg. Chem. Commun.2003, 6, 313. https://doi.org/10.1016/S1387-7003(02)00762-1
  37. Bruker, SHELXTL, Structure Determination Software Programs,Bruker Analytical X-ray Instruments Inc.: Madison, Wisconsin,USA, 1997.
  38. Pan, L.; Thomas, F.; Michelle, B. S.; Huang, X.; Li, J. Inorg.Chem. 2001, 40, 1271. https://doi.org/10.1021/ic001012o
  39. Zaworotko, M. J. Chem. Commun.(feature article) 2001, 1.
  40. Knaust, J. M.; Lopez, S.; Keller, S. W.Inorg. Chim. Acta 2001, 324, 81. https://doi.org/10.1016/S0020-1693(01)00538-2
  41. Bu, X.-H.; Chen, W.; Hou,W.-F.; Du, M.; Zhang, R.-H.; Brisse, F. Inorg. Chem. 2002, 41, 3437. https://doi.org/10.1021/ic020106q
  42. Biradha, K.; Fujita, M. Chem. Commun. 2001, 15, andreferences therein.
  43. Stang, P. J.; Olenyuk, B. Acc. Chem. Res.1997, 30, 502. https://doi.org/10.1021/ar9602011
  44. Suresh, E.; Boopalan, K.; Jasra, R. V.; Bhadbhade, M. M. Inorg.Chem. 2001, 40, 4078. https://doi.org/10.1021/ic000434v
  45. Pschirer, N. G.; Ciurtin, D. M.; Smith, M. D.; Bunz, U. H. F.; zurLoye, H.-C. Angew. Chem., Int. Ed. 2002, 41, 583. https://doi.org/10.1002/1521-3773(20020215)41:4<583::AID-ANIE583>3.0.CO;2-I
  46. Eddaoudi, M.; Kim, J.; Watchter, J. B.; Chae, H. K.; O'Keeffe,M.; Yaghi, O. M. J. Am. Chem. Soc. 2001, 123, 4368. https://doi.org/10.1021/ja0104352
  47. Bourne,S. A.; Lu, J.; Mondal, A.; Moulton, B.; Zaworotko, M. J. Angew.Chem., Int. Ed. 2001, 40, 2111. https://doi.org/10.1002/1521-3773(20010601)40:11<2111::AID-ANIE2111>3.0.CO;2-F
  48. Lu, J.; Mondal, A.; Moulton,B.; Zaworotko, M. J. Angew. Chem., Int. Ed. 2001, 40, 2113. https://doi.org/10.1002/1521-3773(20010601)40:11<2113::AID-ANIE2113>3.0.CO;2-3
  49. Moulton, B.; Lu, J.; Mondal, A.; Zaworotko, M. J. Chem.Commun. 2001, 863.
  50. Cui, Y.; Ngo, H. L.; Lin, W. Inorg. Chem. 2002, 47, 1033.
  51. Chen, B.; Eddaoudi, M.; Reineke, T. M.; Kampf, J. W.; O'Keeffe,M.; Yaghi, O. M. J. Am. Chem. Soc. 2000, 122, 11559. https://doi.org/10.1021/ja003159k

Cited by

  1. Neutral Luminescent Metal-Organic Frameworks: Structural Diversification, Photophysical Properties, and Sensing Applications vol.56, pp.23, 2017, https://doi.org/10.1021/acs.inorgchem.7b02264
  2. Two-dimensional Copper Coordination Polymers Based on Paddle-Wheel Type Secondary Building Units of Cu2(CO2R)4: [Cu(1,3-BDC)(H2O)]·2H2O an vol.25, pp.12, 2003, https://doi.org/10.5012/bkcs.2004.25.12.1955
  3. Synthesis and Magnetic Relaxation of [Mn12O12(O2CCH2CH2CH2Cl)16(H2O)4] Complex vol.25, pp.7, 2003, https://doi.org/10.5012/bkcs.2004.25.7.1036
  4. Hydrothermal Syntheses, Structures, and Properties of Three 3-D Lanthanide Coordination Polymers that Form 1-D Channels vol.2004, pp.14, 2004, https://doi.org/10.1002/ejic.200300876
  5. Doubly-linked 1D coordination polymers derived from 2 ∶ 2 metallamacrocyclic Ni(II) complexes with bipodal acylthiourea and exo-bidentate N-donor bridging ligands: towar vol.29, pp.11, 2005, https://doi.org/10.1039/b509727d
  6. Influence of Angular Dicarboxylate Ligand on the Structures of Single and Double Pillared-Layer Coordination Polymers of Co(II) vol.15, pp.8, 2003, https://doi.org/10.1021/acs.cgd.5b00766