Molecular structure, spectroscopic properties, NLO and NBO analysis of 3,4-Lutidine and [Ag(3,4-Lutidine)2NO3] complex
Tài liệu tham khảo
Chapela, 2003, J. Chem. Crystallogr., 33, 77, 10.1023/A:1023210422362
Percino, 1996, vol. 9
M. Ropars, B. Bloch, French Patent 2 (1974) 261, 296; US Patent 3 S62, 1976.
B.P. Malassine, J.C.C. Gautier, S.H. Chevalier, G.R. Berteleau, US Patent 4163, 1979.
J. Ratto, C.T. Hamermesh, US Patent 4362, 1982.
Azab, 2003, Acta Pharm., 53, 213
Kumar, 2007, Bioorg. Med. Chem., 17, 6459, 10.1016/j.bmcl.2007.09.095
Abdel-Latif, 2007, Monatshefte fur Chemie, 138, 715, 10.1007/s00706-007-0656-8
Amr, 2008, Monatshefte fur Chemie, 139, 1409, 10.1007/s00706-008-0937-x
Amr, 2005, Arch. Pharm. Chem. Life Sci., 338, 433, 10.1002/ardp.200500982
Leonard, 2002, Biol. Pharm. Bull., 25, 215, 10.1248/bpb.25.215
Lourenco, 2007, Arkivoc, 15, 181, 10.3998/ark.5550190.0008.f18
Cocco, 2007, Bioorg. Med. Chem., 15, 1859, 10.1016/j.bmc.2006.11.031
Onnis, 2008, Bioorg. Med. Chem., 16, 2367, 10.1016/j.bmc.2007.11.069
Basnet, 2007, Bioorg. Med. Chem., 15, 4351, 10.1016/j.bmc.2007.04.047
Willemann, 2009, Bioorg. Med. Chem., 17, 4406, 10.1016/j.bmc.2009.05.016
Bahekar, 2007, Bioorg. Med. Chem., 15, 6782, 10.1016/j.bmc.2007.08.005
Singh, 2006, Ind. J. Chem., 45B, 1557
Yar, 2006, Acta Pol. Pharm. Drug Res., 63, 491
Herzigova, 2009, Arch. Pharm. Chem. Life Sci., 342, 394, 10.1002/ardp.200800227
Chavan, 2006, Chem. Heterocycl. Compd., 42, 625, 10.1007/s10593-006-0137-8
Buttelmann, 2003, Bioorg. Med. Chem. Lett., 13, 829, 10.1016/S0960-894X(03)00007-6
Li, 2006, J. Fluorine Chem., 127, 182, 10.1016/j.jfluchem.2005.10.016
Djokic, 2008, ECS Trans., 11, 1, 10.1149/1.2928902
Stillman, 1994, Met.-Based Drugs, 1, 375, 10.1155/MBD.1994.375
Guo, 1999, Angew. Chem. Int. Ed., 38, 1513, 10.1002/(SICI)1521-3773(19990614)38:12<1755::AID-ANIE1755>3.0.CO;2-Q
Ahmad, 2006, Polyhedron, 25, 1633, 10.1016/j.poly.2005.11.004
Legler, 2001, Khim.-Farm. Zh., 35, 501
Kazachenko, 2000, Khim.-Farm. Zh., 34, 257
Criado, 1998, J. Inorg. Biochem., 69, 113, 10.1016/S0162-0134(97)10030-7
Ali, 2001, Polyhedron, 20, 1045, 10.1016/S0277-5387(01)00724-0
McCann, 2003, Polyhedron, 22, 1595, 10.1016/S0277-5387(03)00284-5
Li, 2000, J. Inorg. Biochem., 78, 67, 10.1016/S0162-0134(99)00226-3
Abu-Youssef, 2010, Inorg. Chem., 49, 9788, 10.1021/ic100581k
Abu-Youssef, 2006, Dalton Trans., 2542, 10.1039/B516723J
Abu-Youssef, 2007, Inorg. Chem., 46, 5893, 10.1021/ic0621594
Massoud, 2009, Acta Cryst., C65, 352
Abu-Youssef, 2006, Chem. Commun., 1082, 10.1039/b515399a
Akhavein, 1970, J. Inorg. Nucl. Chem, 32, 1479, 10.1016/0022-1902(70)80634-0
Frisch, 2004
Keith, 2007
M. H. Jamroz, Vibrational Energy Distribution Analysis VEDA 4, Warsaw, 2004–2010.
Bond, 2002, Acta Cryst., E58, o328
Belletete, 2005, J. Phys. Chem. A, 109, 6953, 10.1021/jp051349h
Zhenminga, 2011, Spectrochim. Acta Part A, 78, 1143, 10.1016/j.saa.2010.12.067
Lambert, 1998
Asiria, 2011, Spectrochim. Acta Part A, 82, 44, 10.1016/j.saa.2011.06.058
NIST/EPA Gas-Phase Infrared Database (http://webbook.nist.gov/chemistry).
Destexhe, 1994, J. Phys. Chem., 98, 1506, 10.1021/j100056a023
Scott, 1996, J. Phys. Chem., 100, 16502, 10.1021/jp960976r
Desiraju, 1999
Grabowski, 2004, J. Org. Phys. Chem., 17, 18, 10.1002/poc.685
Pinchas, 1955, Anal. Chem., 27, 2, 10.1021/ac60097a002
Schneider, 1956, Trans. Faraday Soc., 52, 13, 10.1039/tf9565200013
Trudeau, 1980, Top. Curr. Chem., 93, 91, 10.1007/3-540-10058-X_9
Hobza, 2000, Chem. Rev., 100, 4253, 10.1021/cr990050q
Budeŝinsky, 1989, Synthesis, 858, 10.1055/s-1989-27411
Boldeskul, 1997, J. Mol. Struct., 436, 167, 10.1016/S0022-2860(97)00137-3
Gu, 1999, J. Am. Chem. Soc., 121, 9411, 10.1021/ja991795g
Muchall, 2001, J. Phys. Chem. A, 105, 632, 10.1021/jp002984k
Fu, 2003, Spectrochim. Acta Part A, 59, 245, 10.1016/S1386-1425(02)00169-5
Nakamoto, 1997
