References
- Bragg, W. H. The Structure of the Spinel Group of Crystals. Phil. Math. 1915, 30, 305.
- Hahn, T. International Tables for X-ray Crystallography: Space Group Symmetry; 2006; vol. A. chap. 7.1, p 669.
- Nishikawa, S. Proc. Math. Phys. Soc. Tokyo, Japan, 1915, 8, 199.
- O'Neill, H. St. C.; Dollase, W. A. Phys. Chem. Minerals 1994, 20, 541. https://doi.org/10.1007/BF00211850
- Nathawan, P.; Darshane, V. S. Structural J. Phys. 1988, 2, 3191.
- Van der Laag, N. J.; Snel, M. D.; Magusin, P. C. M. M.; De With, G. J. Eur. Cer. Soc. 2004, 24, 2417. https://doi.org/10.1016/j.jeurceramsoc.2003.06.001
- Chen, L.; Horiuchi, T.; Mori, T. Appl. Catal. A. Gen. 2001, 209, 97. https://doi.org/10.1016/S0926-860X(00)00743-2
- Shangguan, W. F.; Teraoka, Y.; Kagawa, S. Appl. Catal. B: Environ. 1996, 8, 217. https://doi.org/10.1016/0926-3373(95)00070-4
- Seiyama, N.; Yamazoe N.; Arai, H. Sensors and Actuators 1983, 4, 85. https://doi.org/10.1016/0250-6874(83)85012-4
- Shioyama, T. K.; Alcohol Dehydratation Employing Zinc Aluminate Catalysis, U.S. Patent Number 4, 260, 845, date of patent 1981.
- Aguilar-Rios, G.; Valenzuela, M.; Salas, P.; Armendariz, M.; Bosh, P.; Del Toro, G.; Silva, R.; Bertin, V.; Castillo, S.; Ramirez-solis, A.; Schifter, I. Appl. Catal. A. Gen. 1995, 127, 65. https://doi.org/10.1016/0926-860X(95)00269-3
- Roesky, R.; Weiguny, J.; Bestgen, H. B.; Dingerdissen, U. Appl. Catal. A: General 1999, 176, 213. https://doi.org/10.1016/S0926-860X(98)00246-4
- Muhammad Abdul Jamal, E.; Sakthi Kumar, D.; Antharaman, M. R. Bull. Mater. Sci. 2011, 34, 251. https://doi.org/10.1007/s12034-011-0071-y
- Sampath, K.; Cordino, F. J. Amer. Ceram. Soc. 1998, 81, 649.
- Hong, W. S.; De Jonghe, L. C. J. Am. Ceram. Soc. 1995, 78, 3217. https://doi.org/10.1111/j.1151-2916.1995.tb07957.x
- Phani, A. R.; Passacantando, M.; Santucci, S. Mater. Chem. Phys. 2001, 68, 66. https://doi.org/10.1016/S0254-0584(00)00270-4
- Hetting, G. F.; Worl, H.; Weiter, H. H. Z. Anorg. Allg. Chem. 1956, 283, 207. https://doi.org/10.1002/zaac.19562830121
- Valenzuela, M. A.; Jacobs, J. P.; Bosch, P.; Reije, S.; Zapata, B.; Brongersman, H. H. Appl. Catal. A: General 1997, 148, 315. https://doi.org/10.1016/S0926-860X(96)00235-9
- Chen, Z.; Shi, E.; Zheng, Y.; Li, W.; Wu, N.; Zhong, W. Mater. Lett. 2002, 56, 601. https://doi.org/10.1016/S0167-577X(02)00561-X
- Biginelli, P. Ber. Dtsch. Chem. Ges. 1891, 24, 2962. https://doi.org/10.1002/cber.189102402126
- Biginelli, P. Gazz. Chim. Ital. 1893, 23, 360.
- Hurst, E. W.; Hull, R. J. Med. Chem. 1961, 3, 215. https://doi.org/10.1021/jm50015a002
- Mayer, T. U.; Kapoor, T. M.; Haggarty, S. J.; King, R. W.; Schreiber, S. I.; Mitchison, T. J. Science 1999, 286, 971. https://doi.org/10.1126/science.286.5441.971
- Kato, T. Jpn. Kokay Tokkyo Koho 1984, 59, 190,974 (CA 102: 132067).
- Atwal, K. S.; Swanson, B. N.; Unger, S. E.; Floyd, D. M.; Moreland, S.; Hedberg, A.; O'Reilly, B. C. J. Med. Chem. 1991, 34, 806. https://doi.org/10.1021/jm00106a048
- Rovnyak, G. C.; Atwal, K. S.; Hedberg, A.; Kimball, S. D.; Moreland, S.; Gougoutas, J. Z.; O'Reilley, B. C.; Schwartz, J.; Malley, M. F. J. Med. Chem. 1992, 35, 3254. https://doi.org/10.1021/jm00095a023
- Kape, C. O. Molecules 1998, 3(1), 1. https://doi.org/10.3390/30100001
- Jauk, B.; Pernat, T.; Kappe, C. O. Molecules 2000, 5, 227. https://doi.org/10.3390/50300227
- Ranu, B. C.; Hajra, A.; Jana, U. J. Org. Chem. 2000, 65, 6270. https://doi.org/10.1021/jo000711f
- Dondoni, A.; Massi, A. Tetrahedron Lett. 2001, 42, 7975. https://doi.org/10.1016/S0040-4039(01)01728-2
- Choudhary, V. R.; Tillu, V. H.; Narkhede, V. S.; Borate, H. B.; Wakhakar, R. D. Catal. Commun. 2003, 4, 449. https://doi.org/10.1016/S1566-7367(03)00111-0
- Stadler, A.; Kappe, C. O. J. Comb. Chem. 2001, 3, 624. https://doi.org/10.1021/cc010044j
- Stadler, A.; Yousefi, B. H.; Dallinger, D.; Walla, P.; Van der Eycken, E.; Kaval, N.; Kappe, C. O. Org. Process Res. Dev. 2003, 7, 707. https://doi.org/10.1021/op034075+
- Lu, L.; Ma, M. Synlett. 2000, 1, 63.
- Lu, L.; Bai, Y. Synthesis 2002, 4, 466.
- Ranu, B. C.; Hajra, A.; Jana, U. J. Org. Chem. 2000, 65, 6270. https://doi.org/10.1021/jo000711f
- Fu, N.-Y.; Yuan, Y.-F.; Cao, Z.; Wang, S. W.; Wang, J.-T.; Peppe, C. Tetrahedron 2002, 58, 4801. 30.
- Fu, N.-Y.; Yuan, Y.-F.; Pang, M.-L.; Wang, J.-T.; Peppe, C. J. Oragnomet. Chem. 2003, 672, 52. https://doi.org/10.1016/S0022-328X(03)00139-6
- Reddy, C. V.; Mahesh, M.; Raju, P. V. K.; Babu, T. R.; Reddy, V. V. N. Tetrahedron Lett. 2002, 43, 2657. https://doi.org/10.1016/S0040-4039(02)00280-0
- Lu, J.; Bay, Y.; Wang, Z.; Yang, B.; Ma, H. Tetrahedron Lett. 2000, 41, 9075. https://doi.org/10.1016/S0040-4039(00)01645-2
- Bose, D. S.; Fatima, L.; Mereyala, H. B. J. Org. Chem. 2003, 68, 587-590. https://doi.org/10.1021/jo0205199
- Quan, Z.-J.; Da, Y.-X.; Zhang, Z.; Wang, X.-C. Catalysis Communication 2009, 10, 1146. https://doi.org/10.1016/j.catcom.2008.12.017
- Gupta, R.; Paul, S.; Gupta, R. Journal of Molecular Catalysis A: Chemica. 2007, 266, 50. https://doi.org/10.1016/j.molcata.2006.10.039
- Sharghi, H.; Jokar, M. Synthetic Communications 2009, 39, 958. https://doi.org/10.1080/00397910802444258
- Xu, H.; Wang, Y-G. Chinese J. Chem. 2003, 21, 327.
- Varala, R.; Alam, M. M.; Adapa, S. R. Synlett. 2003, 67.
- Ma, Y.; Qian, C.; Wang, L.; Yuang, M. J. Org. Chem. 2000, 65, 3864. https://doi.org/10.1021/jo9919052
- Jain, S. L.; Prasad, V. V. D. N.; Sain, B. Catalysis Communications 2008, 9, 499. https://doi.org/10.1016/j.catcom.2007.04.021
- Kantam, M. L.; Ramani, T.; Chakrapani, L.; Choudary, B. M. 2009, 10, 370.
- Barr, T. L.; Seal, S.; Bozniak, K.; Klinowski, J. J. Chem. Soc. Faraday Trans. 1997, 93(1), 181-186. https://doi.org/10.1039/a604061f
- Shirley, D. A. Physical Review B 1972, 5, 4709. https://doi.org/10.1103/PhysRevB.5.4709
- Wagner, C. D., Ed.; Empirically derived atomic sensitivity factor for XPS In: Practical Surface Analysis 1: Auger and X-Ray Spectroscopy; Brings and M. P. Seach, Willey: Chichester 1990; p 635. Appendix 6.
- Altermatt, U. D.; Brown, I. D. Acta Cryst. 1987, A43, 125.
- Zawadzki, M. Sol. State Sci. 2006, 8, 14. https://doi.org/10.1016/j.solidstatesciences.2005.08.006
- JCPDS PDF No 05-0669.
- Shanon, R. D. Acta Cryst. A32 1976, 751.
- Cullity, B. D. Elements of X-Ray Diffraction; Addison-Wesley: London, U.K., 1978; p 101.
- Sigel, G. A.; Bartlett, R. A.; Decker, D.; Olmstead, M. M.; Power, P. P. Inorg. Chem. 1987, 26, 1773. https://doi.org/10.1021/ic00258a028
- Adams, R. W.; Martin, R. L.; Winter, G. Aust. J. Chem. 1970, 20, 773.
- Barraclough, C. G.; Bradley, D. C.; Lewis, J.; Thomas, I. M. J. Chem. Soc. 1961, 2601. https://doi.org/10.1039/jr9610002601
- Ettre, L. S. Pigment Surface, In: Lewis, P. A., Ed.; Pigment Handbook; Wiley-Interscience Publication: Ohio, U.S.A., 1987; p 139.
- Barr, T. L. J. Vac. Sci. Technol. A 1989, 7, 1677. https://doi.org/10.1116/1.576069
- Fritsh, A.; Legare, P. Surf. Sci. 1987, 186, 247. https://doi.org/10.1016/S0039-6028(87)80046-8
- Cocke, D. L.; Johnson, E. D.; Merrill, R. P. Catal. Rev. Sci. Eng. 1984, 26, 163. https://doi.org/10.1080/01614948408078064
- Benoit, R. lasurface, www.Lasurface.com/XPS and AES database.
- Van den Brand, J.; Snijders, P. C.; Sloof, W. G.; Terryn, H.; de Wit, J. H. W. J. Phys. Chem. B 2004, 108, 6017.
- Velu, S.; Suzuki, K.; Vijayaraj, M.; Barmann, S.; Gopinath, C. S. Appl. Catal. 2005, B55, 287.
- Rousseau, S.; Loridant, S.; Delichere, P.; Boreave, A.; Deloume, J. P.; Vernaux, P. Applied Catalysis B: Environmenta 2009, 88, 438. https://doi.org/10.1016/j.apcatb.2008.10.022
- Vincent Crist, B.; XPS international, LLC; PDF Handbooks of Monochromatic XPS Spectra 2005.
- Barr, T. L.; Seal, S.; He, H.; Klinowski, J. Vacuum 1995, 46, 1391. https://doi.org/10.1016/0042-207X(95)00159-X
- Arean, C. O.; Mentrait, M. P.; Lopez, A. J. L.; Parra, J. B. Colloids Surf. A: Physicochem. Engg. Aspects 2001, 180, 253. https://doi.org/10.1016/S0927-7757(00)00590-2
- Salitha, G.; Reddy, G. S. K.; Yadav, J. S. Tetrahedron Lett. 2003, 44, 6497. https://doi.org/10.1016/S0040-4039(03)01564-8
- Amini, M. M.; Shaabani, A.; Bazgir, A. Catal. Commun. 2006, 7, 843. https://doi.org/10.1016/j.catcom.2006.02.027
- Mitra, A. K.; Banerjee, K. Synlett. 2003, 10, 1509.
- Hevari, M. M.; Bakhtiara, K.; Bamoharam, F. Z. Catal. Commun. 2006, 7, 373. https://doi.org/10.1016/j.catcom.2005.12.007
- Russowsky, D.; Lopes, F. A.; Silva, V. S. S.; Canto, K. F. S.; Montes D'Oca, M. G.; Godoi, M. N. J. Braz. Chem. Soc. 2004, 15, 165. https://doi.org/10.1590/S0103-50532004000200002
Cited by
- Decoration of multi-walled carbon nanotubes with NiO nanoparticles and investigation on their catalytic activity to synthesize pyrimidinone heterocycles vol.12, pp.1, 2015, https://doi.org/10.1007/s13738-014-0468-9
- Solvent-free efficient one-pot synthesis of Biginelli and Hantzsch compounds catalyzed by potassium phthalimide as a green and reusable organocatalyst vol.41, pp.8, 2015, https://doi.org/10.1007/s11164-014-1621-x
- 1,3,5-Tris(2-hydroxyethyl)isocyanurate functionalized graphene oxide: a novel and efficient nanocatalyst for the one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones vol.41, pp.14, 2017, https://doi.org/10.1039/C7NJ00632B
- )-ones bearing urea, thiourea, and sulfonylurea moieties pp.1480-3291, 2018, https://doi.org/10.1139/cjc-2018-0239