dc.contributorJournal of Molecular Structure
dc.creatorJohn, Hurtado
dc.creatorLaura, Ibarra
dc.creatorDavid, Yepes
dc.creatorPaola, Garc?a-Huertas
dc.creatorMario, A.Mac?as
dc.creatorOmar, Triana-Chavez
dc.creatorEdgar, Nagles
dc.creatorLeopoldo, Suescun
dc.creatorAlvaro, Mu?oz-Castro
dc.date2023-07-18T23:14:13Z
dc.date2023-07-18T23:14:13Z
dc.date2017-10-15
dc.date.accessioned2023-08-31T19:14:16Z
dc.date.available2023-08-31T19:14:16Z
dc.identifierHurtado, J., Ibarra, L., Yepes, D., Garc?a-Huertas, P., Mac?as, M. A., Triana-Chavez, O., . . . Mu?oz-Castro, A. (2017). Synthesis, crystal structure, catalytic and anti-trypanosoma cruzi activity of a new chromium(III) complex containing bis(3,5-dimethyl
dc.identifierhttps://hdl.handle.net/20.500.12313/3278
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8556612
dc.descriptionThe reaction of CrCl36H2O with the ligand bis(3,5-dimethylpyrazol-1-yl)methane (L) yielded the cationic complex [(Cr(L)(H2O)2Cl2]+, which crystallized as the chloride trihydrate [(Cr(L)(H2O)2Cl2]Cl?3H2O. The chromium complex was characterized by elemental analysis, electrical conductivity, Infrared and Ultraviolet/Visible spectroscopy. The crystal structure determination using single-crystal X-ray diffraction showed a chromium center in a distorted octahedral coordination sphere. In the crystal, the packing was directed by Osingle bondH?(O,Cl) hydrogen bonds and weak Csingle bondH?O interactions to build a monoclinic P21/c supramolecular structure. The complex showed excellent properties as an initiator for the ring opening polymerization of ?-caprolactone (CL) under solvent-free conditions. The obtained polymer showed high crystallinity (89.9%) and a decomposition temperature above 475 ?C. In addition, the new complex was evaluated against epimastigotes from Trypanosoma cruzi (T. cruzi) strains. The results indicated that this complex has a high activity against this parasite with a minimum inhibitory concentration 50 (MIC50) of 1.08 ?g/mL. Interestingly, this compound showed little effect on erythrocytes, indicating that it is not cytotoxic. These results provide interesting contributions to the design of metal complexes by using simple and accessible ligands with activity against T. cruzi and with potential applications in the polymerization of CL.
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dc.languageeng
dc.publisherJournal of Molecular Structure
dc.publisherEstados Unidos de Am?rica
dc.relationhttps://www.sciencedirect.com/science/article/pii/S0022286017307901#cebib0010
dc.relationS. Juli?, P. Sala, J. del Mazo, M. Sancho, C. Ochoa, J. Elguero, J.P. Fayet, M.C. Vertut J. Heterocycl. Chem., 19 (1982), pp. 1141-1145, 10.1002/jhet.5570190531
dc.relationK. Shiu, S. Lin, D. Fung, T. Chan, S. Peng, M. Cheng, J. Chou Inorg. Chem., 34 (1995), pp. 854-863, 10.1021/ic00108a016
dc.relationM. Calhorda, P. Costa, O. Crespo, M. Concepci?n, P. Jones, A. Laguna, M. Naranjo, S. Quintal, Y. Shi, M. Dolores Dalton Trans., 34 (2006), pp. 4104-4113, 10.1039/B605034D
dc.relationJ. Reedijk, J. Verbiest Transit. Mater. Chem., 4 (1979), pp. 239-243, 10.1007/BF00619177
dc.relationM. Bortoluzzi, G. Paolucci, B. Pitteri, A. Vavasori, V. Bertolasi Organometallics, 28 (2009), pp. 3247-3255, 10.1021/om900146a
dc.relationB. Machura, J. Palion, M. Penkala, T. Gron?, H. Duda, R. Kruszynski Polyhedron, 56 (2013), pp. 189-199, 10.1016/j.poly.2013.03.052
dc.relationE. Nagles, L. Ibarra, J. Penagos, J. Hurtado, O. Garc?a-Beltr?n J. Electroanal. Chem., 788 (2017), pp. 38-43, 10.1016/j.jelechem.2017.01.057
dc.relationA. Sandoval-Rojas, L. Ibarra, M. Cort?s, M. Hurtado, M. Mac?as, J. Hurtado Inorg. Chim. Acta, 459 (2017), pp. 95-102, 10.1016/j.ica.2017.01.022
dc.relationJ.C. Wu, T.L. Yu, C.T. Chen, C.C. Lin Coord. Chem. Rev., 250 (2006), pp. 602-626, 10.1016/j.ccr.2005.07.010
dc.relationN.E. Kamber, W. Jeong, R.M. Waymouth, R.C. Pratt, B.G.G. Lohmeijer, J.L. Hedrick Chem. Rev., 107 (2007), pp. 5813-5840, 10.1021/cr068415b
dc.relationC. Obuah, Y. Lochee, O. Zinyemba, J.H.L. Jordaan, D.P. Otto, J. Darkwa J. Mol. Cat. A Chem., 406 (2015), pp. 185-193, 10.1016/j.molcata.2015.05.021
dc.relationD. Appavoo, B. Omondi, I.A. Guzei, J.L. van Wyk, O. Zinyemba, J. Darkwa Polyhedron, 69 (2014), pp. 55-60, 10.1016/j.poly.2013.11.011
dc.relationN. Nu?ez-Dallos, A.F. Posada, J. Hurtado Tetrahedron Lett., 58 (2017), pp. 977-980, 10.1016/j.tetlet.2017.01.088
dc.relationI. Barakat, P. Dubois, R. Jerome, P. Teyssie Macromolecules, 24 (1991), pp. 6542-6545, 10.1021/ma00024a029
dc.relationJ. Li, Y. Deng, S. Jie, Bo-Gen Li J. Organomet. Chem., 797 (2015), pp. 76-82, 10.1016/j.jorganchem.2015.08.002
dc.relationV. Zelen?k, K. Gy?ryov?, D. Mlynarc?k Met.-Based Drugs, 8 (2002), pp. 269-274, 10.1155/MBD.2002.269
dc.relationT.A. Yousef, G.M. Abu EI-Reash, M. Al-Jahdali, EI-Bastawesy R. EI-Rakhawy Spectrochim. Acta Part A, 129 (2014), pp. 163-172, 10.1016/j.saa.2014.02.184
dc.relationR.S. Corr?a, M.M. da Silva, A.E. Graminha, C.S. Meira, J.A.F. dos Santos, D.R.M. Moreira, M.B.P. Soares, G. Von Poelhsitz, E.E. Castellano, C. Bloch Jr., M.R. Cominetti, A.A. Batista J. Inorg. Biochem., 156 (2016), pp. 153-163, 10.1016/j.jinorgbio.2015.12.024
dc.relationL.R. Gouvea, D.A. Martins, D da Gama Jean Batista, Maria de Nazar? C. Soeiro, Sonia R.W. Louro, Paulo J.S. Barbeira, Let?cia R. Teixeira Biometals, 26 (2012), pp. 813-825, 10.1007/s10534-013-9661-z
dc.relationK. Castillo, N. Bello-Vieda, N. Nu?ez-Dallos, H. Pastrana, A. Celis, S. Restrepo, J. Hurtado, A. ?vila J. Braz. Chem. Soc., 27 (2016), pp. 2334-2347, 10.5935/0103-5053.20160130
dc.relationL.C. Dias, M.A. Dessoy, J.J.N. Silva, O.H. Thiemann, G. Oliva, A.D. Andricopulo Qu?m. Nova, 32 (2009), pp. 2444-2457, 10.1590/S0100-40422009000900038
dc.relationI. Machado, S. Fern?ndez, L. Becco, B. Garat, J.S. Gancheff, A. Rey, D. Gambino J. Coord. Chem., 67 (2014), pp. 1835-1850, 10.1080/00958972.2014.926008
dc.relationM.N.C. Soeiro, S.L. de Castro Expert Opin. Ther. Targets, 13 (2009), pp. 105-121, 10.1517/14728220802623881
dc.relationB. Demoro, F. Caruso, M. Rossi, D. Ben?tez, M. Gonz?lez, H. Cerecetto, M. Galizzi, L. Malayil, R. Docampo, R. Faccio, A.W. Mombr?, D. Gambino, L. Otero Dalton Trans., 41 (2012), pp. 6468-6476, 10.1039/c2dt12179d
dc.relationJ.J.N. Silva, A.L. Osakabe, W.R. Pavanelli, J.S. Silva, D.W. Franco Br. J. Pharmacol., 152 (2007), pp. 112-121, 10.1038/sj.bjp.0707363
dc.relationE. Rodriguez, C. Sarniguet, T.S. Morales, M. Vieites, A.I. Tomaz, A. Medeiros, M.A. Comini, J. Varela, H. Cerecetto, M. Gonz?lez, F. Marques, M.H. Garc?a, L. Otero, D. Gambino J. Coord. Chem., 68 (2015), pp. 2923-2937, 10.1080/00958972.2015.1062480
dc.relationJ.J. Nogueira, W.R. Pavanelli, F.R. Salazar, F.C. Alves, A.B. Ferreira da Silva, J.S. Silva, D.W. Franco J. Med. Chem., 51 (2008), pp. 4104-4114, 10.1021/jm701306r
dc.relationZ.K.Q. Ferreira, E. Tfouni J. Braz. Chem. Soc., 21 (2010), pp. 1349-1358, 10.1590/S0103-50532010000700022
dc.relationD.A. Martins, L.R. Gouvea, G.S. Vignoli Muniz, S.R.W. Louro, Denise da Gama Jaen Batista, Maria de Nazar? C. Soeiro, L.R. Teixeira Bioinorg. Chem. Appl., 2016 (2016), pp. 1-11, 10.1155/2016/5027404
dc.relationD.A. Martins, L.R. Gouvea, Denise da Gama Jean Batista, P. B. da Silva, S.R.W. Louro, Maria de Nazar? C. Soeiro, L.R. Teixeira Biometals, 25 (2012), pp. 951-960, 10.1007/s10534-012-9565-3
dc.relationJ. Jeeva, T. Ramachandramoorthy Res. J. Pharm. Sci., 2 (2013), pp. 1-6
dc.relationM. Thomas, A. Kulandaisamy, A. Manohar Int. J. ChemTech. Res., 4 (2012), pp. 247-257
dc.relationChang-Xue An, Xin-Li Han, Peng-Bang Wang, Zhi-Hui Zhang, Hai-Ke Zhang, Zhi-Jin Fan Transit. Mater. Chem., 33 (2008), pp. 835-841, 10.1007/s11243-008-9119-2
dc.relationA. Boni, G. Pampaloni, R. Peloso, D. Belletti, C. Graiff, A. Tiripicchio J. Organomet. Chem., 691 (2006), pp. 5602-5609, 10.1016/j.jorganchem.2006.09.006
dc.relationN.G. Park, U. Silphaduang, H.S. Moon, J.K. Seo, J. Corrales, E.J. Noga Biochemistry, 50 (2011), pp. 3288-3299, 10.1021/bi101395j
dc.relationG. Socrates Infrared and Raman Characteristic Group Frequencies: Tables and Charts (third ed.), John Wiley & Sons, Chichester (2004)
dc.relationJ. Hurtado, N. Nu?ez-Dallos, S. Movilla, G.P. Miscione, B.C. Peoples, R. Rojas, M. Valderrama, R. Fr?hlich J. Coord. Chem., 70 (2017), pp. 803-818, 10.1080/00958972.2017.1286330
dc.relationJ.C.A. Boeyens J. Cryst. Mol. Struct., 8 (1978), pp. 317-320, 10.10.1007/bf012004851
dc.relationD. Cremer, J. Pople J. Am. Chem. Soc., 97 (1975), pp. 1354-1358, 10.1021/ja00839a011
dc.relationM. Zheng, H. Wu, X. Zhang, J. Zhang J. Organomet. Chem., 817 (2016), pp. 21-25, 10.1016/j.jorganchem.2016.04.033
dc.relationJ. Zhang, A. Li, T.S. Andy Hor Dalton Trans., 42 (2009), pp. 9327-9333, 10.1039/B909685J
dc.relationL. Tang, Z. Wang, J. Chai, J. Wang J. Chem. Crystallogr., 32 (2002), pp. 261-265, 10.1023/A:1020205224041
dc.relationG. te Velde, F.M. Bickelhaupt, E.J. Baerends, C. Fonseca Guerra, S.J.A. van Gisbergen, J.G. Snijders, T. Ziegle J. Comput. Chem., 22 (2001), pp. 931-967, 10.1002/jcc.1056
dc.relationJ.P. Perdew, K. Burke, M. Ernzerhof Phys. Rev. Lett., 77 (1996), pp. 3865-3868, 10.1103/PhysRevLett.77.3865
dc.relationS. Grimme Interdiscip. Rev. Comput. Mol. Sci., 1 (2011), pp. 211-228, 10.1002/wcms.30
dc.relationJ. Contreras-Garc?a, E.R. Johnson, S. Keinan, R. Chaudret, J.P. Piquemal, D.N. Beratan, W. Yang J. Chem. Theory Comput., 7 (2011), pp. 625-632, 10.1021/ct100641a
dc.relationG. Saleh, C. Gatti, L. Lo Presti Comput. Theory Chem., 998 (2012), pp. 148-163, 10.1016/j.comptc.2012.07.014
dc.relationT. Ziegler, A. Rauk Theory Chim. Acta, 46 (1977), pp. 1-10, 10.1007/BF02401406
dc.relationM. Xue, R. Jiao, Y. Zhang, Y. Yao, Q. Shen Eur. J. Inorg. Chem., 27 (2009), pp. 4110-4118, 10.1002/ejic.200900313
dc.relationA. Otero, J. Fern?ndez-Baeza, A. Anti?olo, A. Lara-S?nchez, E. Mart?nez-Caballero, J. Tejeda, L.F. S?nchez- Barba, C. Alonso-Moreno, I. L?pez-Solera Organometallics, 27 (2008), pp. 976-983, 10.1021/om701033r
dc.relationJ. Hurtado, R. Rojas, M. Valderrama Rev. Invest. Univ. Quind?o. Col., 24 (2013), pp. 8-16
dc.relationK. Phillipson, M. Jenkins, J. Hay J. Therm. Anal. Calorim., 123 (2016), pp. 1491-1500, 10.1007/s10973-015-5047-5
dc.relationM. Labet, W. Thielemans Chem. Soc. Rev., 38 (2009), pp. 3484-3504, 10.1039/b820162p
dc.relationZ. Gu, L. Li, Q. Bao, F. Yuan Chin. J. Chem., 33 (2015), pp. 563-567, 10.1002/cjoc.201400826
dc.relationQ. Guo, G. Groeninckx Polymer, 42 (2001), pp. 8647-8655, 10.1016/S0032-3861(01)00348-2
dc.relationD.H. Weinkauf, D.R. Paul ACS Symp. Ser., 423 (1990), pp. 60-91, 10.1021/bk-1990-0423.ch003
dc.relationH. Van den Bossche, G. Willemsens, W. Cools, P. Marichal, W. Lauwers Biochem. Soc. Trans., 11 (1983), pp. 665-667, 10.1042/bst0110665
dc.relationR. Herbrecht Expert Rev. Anti Infect. Ther., 2 (4) (2004), pp. 485-497
dc.relationD.A. Heerding, G. Chan, W.E. DeWolf, A.P. Fosberry, C.A. Janson, D.D. Jaworski, E. McManus, W.H. Miller, T.D. Moore, D.J. Payne, X. Qiu, S.F. Rittenhouse, C. Slater-Radosti, W. Smith, D.T. Takata, K.S. Vaidya, C.C.K. Yuan, W.F. Huffman Bioorg. Med. Chem. Lett., 11 (2001), p. 2061, 10.1016/S0960-894X(01)00404-8
dc.relationYan Wang, Guri L.V. Damu, Jing-Song Lv, Rong-Xia Geng, Da-Cheng Yang, Chen-He Zhou Bioorg. Med. Chem. Lett., 22 (2012), pp. 5363-5366, 10.1016/j.bmcl.2012.07.064
dc.relationN.K. Singh, S.B. Singh, D.K. Singh, V.B. Chauhan Indian J. Chem. Sec A, 42A (2003), pp. 2767-2771
dc.relationR. Ferreira, M. de Melo, M. Moraes Junior, L. Ferreira Braz. J. Med. Biol. Res., 21 (1988), pp. 1069-1077
dc.relationA. Buschini, L. Ferrarini, S. Franzoni, S. Galati, M. Lazzaretti, F. Mussi, C. Northfleet de Albuquerque, T. Maria Araujo Domingues Zucchi, P. Poli J. Parasitol. Res., 463575 (2009), pp. 1-11, 10.1155/2009/463575
dc.relationM.A. Raj?o, C. Furtado, C.L. Alves, D.G. Passos-Silva, M. Barbi de Moura, B.L. Schamber-Reis, M. Kunrath-Lima, A. Ara?jo Zuma, J.P. Vieira-da-Rocha, J.B. Ferreira Garcia, I.C. Mendes, S.D. Junho Pena, A.M. Macedo, G.R. Franco, N.C. de Souza-Pinto, M.H. Gennari de Medeiros, A.K. Cruz, M.C. Machado Motta, S.M. Ribeiro, C.R. Machado Environ. Mol. Mutagen, 55 (2014), pp. 309-321, 10.1002/em.21839
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dc.sourcehttp://www.sciencedirect.com/science/article/pii/S0022286017307901
dc.subjectChromium complex
dc.subjectCrystal structure
dc.subjectRing opening polymerization
dc.subject?-caprolactone
dc.subjectTrypanosoma cruzi
dc.subjectChromium complex
dc.subjectCrystal structure
dc.subjectRing opening polymerization
dc.subject?-caprolactone
dc.subjectTrypanosoma cruzi
dc.subjectChromium complex
dc.subjectCrystal structure
dc.subjectRing opening polymerization
dc.subject?-caprolactone
dc.subjectTrypanosoma cruzi
dc.titleSynthesis, crystal structure, catalytic and anti-Trypanosoma cruzi activity of a new chromium(III) complex containing bis(3,5-dimethylpyrazol-1-yl)methane
dc.typeArticle
dc.typehttp://purl.org/coar/resource_type/c_6501
dc.typehttp://purl.org/coar/version/c_970fb48d4fbd8a85
dc.typeText
dc.typeinfo:eu-repo/semantics/article
dc.typehttp://purl.org/redcol/resource_type/ARTOTR
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