14. Altun Ah., Kumru M., Dimoglo A. (2001), “Study of electronic and structural features of thiosemicacbazon and thiosemicarbazide derivatives demonstrating anti-HSV-1 activity”, J. Mol. Struct., 535, 235-246.
15. Arduengo J. III., Harlow R. L., M. Kline (1991), “A stable crystalline carbene”, J. Am. Chem. Soc., 113, 361-363.
16. Arghya B., Copal Das. (2011), “Zn(II) and Hg(II) complexes of naphthalene based thiosemicacbazon Structure and spectroscopic studies”, Inorganica Chim. Acta, 372, 394-399.
17. Boubakri L., Yasar S., Dorcet V., Roisnel T., Bruneau C., Hamdi N., Ozdemir I. (2017), “Synthesis and catalytic applications of palladium N- heterocyclic carbene complexes as efficient pre-catalysts for Suzuki-Miyaura and Sonogashira coupling reactions”, New J. Chem., 41(12), 5105-5113.
18. Demertzi D. K., Domopoulou A., Demertzis M. A., Valle G., Papageorgiou A. (1997), “Palladium(II) complexes of 2-acetylpyridine N(4)-methyl, N(4)- ethyl and N(4)-phenyl-thiosemicacbazons. Crystal structure of chloro(2- acetylpyridine N(4)-methylthiosemicacbazonato) palladium(II). Synthesis,
spectral studies, in vitro and in vivoantitumour activity”, J. Inorg. Biochem., 68, 147–155.
19. El-Asmy A.A., Morsi M.A., El-Shafei A.A. (2005), “Cobalt(II), nickel(II), copper(II), zinc(II) and uranyl(VI) complexes of acetylacetone bis(4- phenylthiosemicacbazon)”, Transit. Met. Chem, 11, 494-496.
20. Frenking G., Solà M., Vyboishchikov S. F. (2005), “Chemical bonding in transition metal carbene complexes”, J. Organomet. Chem., 690, 6178-6204.
21. Gray H. B., Ballhausen C. J. (1962), “A molecular orbital theory for square planar metal complexes”, J. Am. Chem. Soc, 85, 260-265.
22. Hahn F. E., Jahnke M. C. (2008), “Heterocyclic carbenes: synthesis and coordination chemistry”, Angew. Chem. Int. Ed. Engl., 47(17), 3122-3172.
23. Herrmann W. A., Kocher C. (1997), “N-Heterocyclic Carbenes”, Angew.
Chem. Int. Ed. Engi., 36, 2162-2187.
24. Herrmann W.A. (2002), “N-heterocyclic carbenes: a new concept in organometallic catalysis”, Angew. Chem., Int. Ed. Engl., 41(8), 1290-1309 25. Hindi K. M., Panzner M. J., Tessier C. A., Cannon C. L., Youngs W. J.
(2009), “The Medicinal Applications of Imidazolium Carbene Metal Complexes”, Chem. Rev. 2009, 109(8), 3859-3884.
26. Hueting R., Tavaré R., Dilworth J. R., Mullen G. E. (2013), “Copper-64 radiolabelling of the C2A domain of synaptotagmin I using a functionalised bis(thiosemicacbazon): A pre- and post-labelling comparison”, J. Inorg.
Biochem., 128C, 108-111.
27. Huynh H. V. (2017), The Organometallic Chemistry of N-heterocyclic CarbenesThe Organometallic Chemistry of N-heterocyclic Carbenes, Wiley.
28. Huynh H. V. (2018), “Electronic Properties of N-Heterocyclic Carbenes and Their Experimental Determination”, Chem. Rev. 2018, 118(19), 9457-9492.
29. Huynh H. V., Han Y., Jothibasu R., Yang J. A. (2009), “13C NMR Spectroscopic Determination of Ligand Donor Strengths Using N-
Heterocyclic Carbene Complexes of Palladium(II)”, Organometallics 2009, 28, 5395-5404.
30. Ivan J.B.Lin, SekharVasam C. (2007), “Preparation and application of N- heterocyclic carbene complexes of Ag(I)”, Coord. Chem. Rev., 251, 642-67.
31. Jacobsen H., Correa A., Poater A., Costabile C., Cavallo L. (2009),
“Understanding the M – (NHC) (NHC = N-heterocyclic carbene) bond”, Coord. Chem. Rev., 253, 687-703.
32. Kluger R. (1987), “Thiamin diphosphate: a mechanistic update on enzymic and nonenzymic catalysis of decarboxylation”, Chem. Rev., 87(5), 863-876.
33. Kửcher C., Herrmann W. A. (1997), “Heterocyclic carbenes. One-pot synthesis of rhodium and iridium carbene complexes”, J. Organomet. Chem., 532, 261-265.
34. Li K., Zou T., Chen Y., Guan X., & Che C. M. (2015), “Pincer-Type Platinum(II) Complexes Containing N-Heterocyclic Carbene (NHC) Ligand:
Structures, Photophysical and Anion-Binding Properties, and Anticancer Activities”, Chem. Eur. J., 21(20), 7441–7453.
35. Lin J. C. Y., Huang R. T. W., Lee C. S., Bhattacharyya A., Hwang W. S., Lin I. J. B. (2009), “Coinage Metal−N-Heterocyclic Carbene Complexes”, Chem. Rev., 109, 8, 3561-3598.
36. Mahajan R. K., Walia T. P., Sumanjit, Labana T. S. (2005), “The versatility of salicylaldehyde thiosemicacbazon in the determination of copper in blood using adsorptives tripping voltammetry”, Talanta, 67, pp. 755 - 759.
37. Nguyen V. H., El Ali B. M., Huynh H. V. (2018), “Stereoelectronic Flexibility of Ammonium-Functionalized TriazoleDerived Carbenes:
Palladation and Catalytic Activities in Water”, Organometallics 2018, 37, 2358−2367.
38. Palanimuthu D., Samunelson A. G. (2013), “Dinuclear Zinc bis(thiosemicacbazon) complexes, in vitro anticancer activity, cellular uptake and AND interaction study”, Inorganica Chim. Acta, 408, 152-161.
39. Patel H. D., Divatia S. M., Clercq E. de (2013), “Synthesis of some novel thiosemicacbazon derivatives having anti-cancer, anti-HIV as well as anti- bacterial activity”, Indian J. Chem., 52B, 535-545.
40. Prabhu R. N., Ramesh R. (2012), “Catalytic application of dinuclear palladium(II) bis(thiosemicacbazon) complex in the Mizoroki-Heck reaction”, Tetrahedron Lett., 53, 5961–5965.
41. Prabhu R. N., Ramesh R. (2013), “Synthesis and structural characterization of palladium(II) thiosemicacbazon complex: application to the Buchwald–
Hartwig amination reaction”, Tetrahedron Lett., 54, 1120–1124.
42. Ramana Murthy G. V., Sreenivasulu Reddy T. (1992), 'O- Hydroxyacetophenone thiosemicarbazone as a reagent for the rapid spectrophotometric determination of palladium", Talanta, 39(6), 976-701.
43. Rana B. K., Seth S. K., Bertolasi V. (2015), “Pd(II) – N- heterocyclic carbene complexes of annelated ligand: Synthesis, characterization, and catalytic activity”, Inorganica Chim. Acta, 438, 58-63.
44. Schuster G. B. (1986), “Structure and reactivity of carbenes having aryl substituents”, Adv. Phys. Org. Chem., 22, 311.
45. Shipman C. Jr., Smith S. H., Drach J. C., Klayman D. L. (1981), “Antiviral Activity of 2-Acetylpyridine Thiosemicacbazons Against Herpes Simplex Virus”, Antimicrob. Agents Chemother., 19(4), 682-685.
46. Singh M. S. (2014), Reactive Intermediates in Organic Chemistry: Structure, Mechanism, and Reactions, Wiley VCH.
47. Suganthy P.K., Prabhu R. N., Sridevi V. S. (2013), “Nickel(II) thiosemicacbazon complex catalyzed Mizoroki–Heck Reaction”, Tetrahedron Lett., 54, 5695–5698.
48. Sun R. W. Y., Chow A. L. F., Li X. H., Yan J. J., Chui S. S. Y., Che C. M.
(2011), “Luminescent cyclometalated platinum(II) complexes containing N- heterocyclic carbene ligands with potent in vitro and in vivo anti-cancer
properties accumulate in cytoplasmic structures of cancer cells”, Chem. Sci., 2(4), 728–736.
49. Teng Q., Huynh H. V. (2014), “Determining the Electron-Donating Properties of Bidentate Ligands by 13C NMR Spectroscopy”, Inorg. Chem., 53, 20, 10964-10973.
50. Teng Q., Huynh H. V. (2017), “A unified ligand electronic parameter based on 13C NMR spectroscopy of N Heterocyclic carbene complexes”, ‐ Dalton Trans., 46(3), 614-627.
51. Vinuelas-Zahínos E., Luna-Giles F., Torres-García P., Fernández-Calderón M. C. (2011), “Co(III), Ni(II), thiosemicacbazon: activity”, Eur. J. Med.
Chem., 46, 150-159.
52. Wang H. M. J., Lin I. J. B. (1998), “Facile Synthesis of Silver(I)−Carbene Complexes. Useful Carbene Transfer Agents”, Organometallics, 17, 5, 972- 975.
53. Yan X., Feng R., Yan C., Lei P., Guo S., Huynh H. V. (2018), “A palladacyclic N-heterocyclic carbene system used to probe the donating abilities of monoanionic chelators”, Dalton Trans., 47(23), 7830-7838.
54. Yuan D., Huynh H. V. (2012), “1,2,3-Triazolin-5-ylidenes: Synthesis of Hetero-bis(carbene) Pd(II) Complexes, Determination of Donor Strengths, and Catalysis”, Organometallics 2012, 31, 1, 405-412.