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How to cite this paper
APA: Mallah, E., Sweidan, K., Abu-Qatouseha, L., Arafat, T & Joshi, R. (2020). Synthesis and Characterization of Some Derivatives of 1,3-Diisopropyl-4,5-dimethylimidazol-2-ylidene. Current Chemistry Letters, 9(4), 199-204.
Chicago/Turabian: Mallah, E., Sweidan, K., Abu-Qatouseha, L., Arafat, T & Joshi, R. 2020. "Synthesis and Characterization of Some Derivatives of 1,3-Diisopropyl-4,5-dimethylimidazol-2-ylidene." Current Chemistry Letters 9, no. 4 (2020): 199-204.
AMA: Mallah, E., Sweidan, K., Abu-Qatouseha, L., Arafat, T & Joshi, R. Synthesis and Characterization of Some Derivatives of 1,3-Diisopropyl-4,5-dimethylimidazol-2-ylidene. Current Chemistry Letters. 2020;9(4):199-204.
References
1. Ott, I. (2017) Medicinal chemistry of metal N-heterocyclic carbene (NHC) complexes. Inorganic and Organometallic Transition Metal Complexes with Biological Molecules and Living Cells. Academic Press, 147-179.
2. Bellemin-Laponnaz, S., Despagnet-Ayoub, E., Díez-González, S., Gade, L. H., Glorius, F., Louie, J., Nolan, S. P., Peris, E., Ritter, T., Rogers, M. M. and Stahl, S. S. (2004) N-Heterocyclic carbenes in transition metal catalysis. Top. Organomet. Chem., 21.
3. Smith, C. A., Narouz, M. R., Lummis, P. A., Singh, I., Nazemi, A., Li, C. H. and Crudden, C. M. (2019) N-Heterocyclic carbenes in materials chemistry. Chem. Rev., 119 (8), 4986-5056.
4. Dayyih, W. A., Mallah, E., Sweidan, K., Al-Sheikh, A. and Steimann, M. (2013) Crystal structure of 1, 3-diisopropyl-4, 5-dimethylimidazolium oxalic acid monomethyl ester, C14H24N2O4. Z. Krist.-New Cryst. St., 228 (1), 55-56.
5. Kuhn, N., Richter, M., Steimann, M., Ströbele, M. and Sweidan, K. (2004) Hydrogen bonding in imidazolium ntrates [1]. Z. Anorg. Allg. Chem., 630 (12), 2054-2058.
6. Kuhn, N., Steimann, M. and Sweidan, K. (2005) The crystal structure of 1, 3-dicyclohexyl-4, 5-dimethylimidazolium dicyanomethylide. Z. Naturforsch. B 1(1), 123-124.
7. Kuhn, N., Abu-Rayyan, A., Al-Sheikh, A., Eichele, K., Maichle-Moßmer, C., Steimann, M. and Sweidan, K. (2005) The structural chemistry of 2-methylenimidazolines (In German). Z. Naturforsch., 1(3), 294-299.
8. Doser, B., Sweidan, K., Kuhn, N. and Ochsenfeld, C. (2015) Unexpected dimerization of 1,3‐dimethyl‐5‐methylenebarbituric acid revealed by a combined experimental and computational study. J. Phys. Org. Chem., 28 (5), 354-357.
9. Wasserscheid, P. and Keim, W. (2000) Ionic liquids—new “solutions” for transition metal catalysis. Angew. Chem. Int. Edit., 39 (21), 3772-3789.
10. Canal, J. P., Ramnial, T., Dickie, D. A. and Clyburne, J. A. (2006) From the reactivity of N-heterocyclic carbenes to new chemistry in ionic liquids. Chem. Commun., (17), 1809-1818.
11. Kuhn, N. and Kratz, T. (1993) Synthesis of imidazol-2-ylidenes by reduction of imidazole-2-(3H)-thiones. Synthesis (Stuttgart), (6), 561-562.
12. Talavera, G., Pena, J., and Alcarazo, M. (2015) Dihalo (imidazolium) sulfuranes: A versatile platform for the synthesis of new electrophilic group-transfer reagents. J. Am. Chem. Soc., 137 (27), 8704-8707.
13. Harpp, D. N., and Smith, R. A. (1982) Organic sulfur chemistry. 42. Sulfur-sulfur bond cleavage processes. Selective desulfurization of trisulfides. J. Am. Chem. Soc., 104 (22), 6045-6053.
14. Dayyih, W. A., Mallah, E., Sweidan, K., Al-Sheikh, A., and Steimann, M. (2013) Crystal structure of 1, 3-diisopropyl-4, 5-dimethylimidazolium oxalic acid monomethyl ester, C14H24N2O4. Z. Krist.-New Cryst. St., 228 (1), 55-56.
15. Mizuuchi, H., Jaitely, V., Murdan, S., and Florence, A. T. (2008) Room temperature ionic liquids and their mixtures: potential pharmaceutical solvents. Eur. J. Pharm. Sci., 33 (4-5), 326-331.
16. MacDougall, D. J., Kennedy, A. R., Noll, B. C., and Henderson, K. W. (2005) Synthesis of mono-and geminaldimetalatedcarbanions of bis (phenylsulfonyl) methane using alkali metal bases and structural comparisons with lithiatedbis (phenylsulfonyl) imides. Dalton T., (12), 2084-2091.
17. Abu-Rayyan, A., Abu-Salem, Q., Mallah, E., Maichle-Mößmer, C., Steimann, M., Norbert Kuhn, N. and Zeller, K. (2008) The Acetylacetonate ion as its E/Z-isomer in 1,3-diisopropyl-4,5- dimethylimidazolium acetylacetonate. Z. Naturforsch. B 63 (12), 1438-1440.
1. Ott, I. (2017) Medicinal chemistry of metal N-heterocyclic carbene (NHC) complexes. Inorganic and Organometallic Transition Metal Complexes with Biological Molecules and Living Cells. Academic Press, 147-179.
2. Bellemin-Laponnaz, S., Despagnet-Ayoub, E., Díez-González, S., Gade, L. H., Glorius, F., Louie, J., Nolan, S. P., Peris, E., Ritter, T., Rogers, M. M. and Stahl, S. S. (2004) N-Heterocyclic carbenes in transition metal catalysis. Top. Organomet. Chem., 21.
3. Smith, C. A., Narouz, M. R., Lummis, P. A., Singh, I., Nazemi, A., Li, C. H. and Crudden, C. M. (2019) N-Heterocyclic carbenes in materials chemistry. Chem. Rev., 119 (8), 4986-5056.
4. Dayyih, W. A., Mallah, E., Sweidan, K., Al-Sheikh, A. and Steimann, M. (2013) Crystal structure of 1, 3-diisopropyl-4, 5-dimethylimidazolium oxalic acid monomethyl ester, C14H24N2O4. Z. Krist.-New Cryst. St., 228 (1), 55-56.
5. Kuhn, N., Richter, M., Steimann, M., Ströbele, M. and Sweidan, K. (2004) Hydrogen bonding in imidazolium ntrates [1]. Z. Anorg. Allg. Chem., 630 (12), 2054-2058.
6. Kuhn, N., Steimann, M. and Sweidan, K. (2005) The crystal structure of 1, 3-dicyclohexyl-4, 5-dimethylimidazolium dicyanomethylide. Z. Naturforsch. B 1(1), 123-124.
7. Kuhn, N., Abu-Rayyan, A., Al-Sheikh, A., Eichele, K., Maichle-Moßmer, C., Steimann, M. and Sweidan, K. (2005) The structural chemistry of 2-methylenimidazolines (In German). Z. Naturforsch., 1(3), 294-299.
8. Doser, B., Sweidan, K., Kuhn, N. and Ochsenfeld, C. (2015) Unexpected dimerization of 1,3‐dimethyl‐5‐methylenebarbituric acid revealed by a combined experimental and computational study. J. Phys. Org. Chem., 28 (5), 354-357.
9. Wasserscheid, P. and Keim, W. (2000) Ionic liquids—new “solutions” for transition metal catalysis. Angew. Chem. Int. Edit., 39 (21), 3772-3789.
10. Canal, J. P., Ramnial, T., Dickie, D. A. and Clyburne, J. A. (2006) From the reactivity of N-heterocyclic carbenes to new chemistry in ionic liquids. Chem. Commun., (17), 1809-1818.
11. Kuhn, N. and Kratz, T. (1993) Synthesis of imidazol-2-ylidenes by reduction of imidazole-2-(3H)-thiones. Synthesis (Stuttgart), (6), 561-562.
12. Talavera, G., Pena, J., and Alcarazo, M. (2015) Dihalo (imidazolium) sulfuranes: A versatile platform for the synthesis of new electrophilic group-transfer reagents. J. Am. Chem. Soc., 137 (27), 8704-8707.
13. Harpp, D. N., and Smith, R. A. (1982) Organic sulfur chemistry. 42. Sulfur-sulfur bond cleavage processes. Selective desulfurization of trisulfides. J. Am. Chem. Soc., 104 (22), 6045-6053.
14. Dayyih, W. A., Mallah, E., Sweidan, K., Al-Sheikh, A., and Steimann, M. (2013) Crystal structure of 1, 3-diisopropyl-4, 5-dimethylimidazolium oxalic acid monomethyl ester, C14H24N2O4. Z. Krist.-New Cryst. St., 228 (1), 55-56.
15. Mizuuchi, H., Jaitely, V., Murdan, S., and Florence, A. T. (2008) Room temperature ionic liquids and their mixtures: potential pharmaceutical solvents. Eur. J. Pharm. Sci., 33 (4-5), 326-331.
16. MacDougall, D. J., Kennedy, A. R., Noll, B. C., and Henderson, K. W. (2005) Synthesis of mono-and geminaldimetalatedcarbanions of bis (phenylsulfonyl) methane using alkali metal bases and structural comparisons with lithiatedbis (phenylsulfonyl) imides. Dalton T., (12), 2084-2091.
17. Abu-Rayyan, A., Abu-Salem, Q., Mallah, E., Maichle-Mößmer, C., Steimann, M., Norbert Kuhn, N. and Zeller, K. (2008) The Acetylacetonate ion as its E/Z-isomer in 1,3-diisopropyl-4,5- dimethylimidazolium acetylacetonate. Z. Naturforsch. B 63 (12), 1438-1440.