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BY-NC-ND 3.0 license Open Access Published by De Gruyter Open Access October 28, 2008

A novel triply bridged dinuclear four-coordinate copper(I) complex with sterically bulky bis(dicyclohexylphosphino)methane ligand

  • Zu-Fu Yao EMAIL logo , Xin Gan and Wen-Fu Fu
From the journal Open Chemistry

Abstract

A novel triply bridged dinuclear copper(I) complex: Cu2(μ-paa)(μ-dcpm)2(BF4)2·2CH2Cl2 [ paa = pyridine-2-carbaldehyde azine (C12H10N4) and dcpm = bis(dicyclohexylphosphino)methane(C25H46P2) ] has been synthesized and structurally characterized. Crystallographic studies of the complex showed that two copper(I) ions were bridged by one paa ligand and two dcpm ligands. The paa ligand adopted the Z configuration at the partially double N-N bond and the two copper ions have distorted tetrahedral coordination geometry. Because of the steric effect of dcpm, the pyridine rings of the paa ligand are obviously not on the same plane (the dihedral angle is 43.610). The interaction between neighboring ligands results in a N-N bond length (1.374(7) Å) contraction. The UV-vis spectra of the complex exhibited intense high-energy absorptions at λmax

[1] K. Kalyanasundaram, M. Gratzel (Eds.): Photosensitization and Photocatalysis using Inorganic and Organometallic Compounds (Kluwer Academic, Dordrecht, 1993) 10.1007/978-94-017-2626-9Search in Google Scholar

[2] A. Juris, V. Balzani, F. Barigelletti, S. Campagna, P. Belser and A. V. Zelewsky, Coordin. Chem. Rev. 84, 85 (1988) http://dx.doi.org/10.1016/0010-8545(88)80032-810.1016/0010-8545(88)80032-8Search in Google Scholar

[3] V.W.W. Yam and K.K.W. Lo, Chem. Soc. Rev. 28, 323 (1999) http://dx.doi.org/10.1039/a804249g10.1039/a804249gSearch in Google Scholar

[4] J. Granifo, A. Vega and M.T. Garland, Polyhedron 17, 1729 (1998) http://dx.doi.org/10.1016/S0277-5387(97)00464-610.1016/S0277-5387(97)00464-6Search in Google Scholar

[5] D.A. Edwards, G.M. Hoskins, M.F. Mahon, K.C. Malloy and G.R.G. Rudolph, Polyhedron 17, 2321 (1998) http://dx.doi.org/10.1016/S0277-5387(97)00533-010.1016/S0277-5387(97)00533-0Search in Google Scholar

[6] J. Granifo, M.E. Vargas, E.S. Dodsworth, D.H. Farrar, S.S. Fielder and A. B. P. Lever, J. Chem. Soc., Dalton Trans. 4369 (1996) 10.1039/dt9960004369Search in Google Scholar

[7] M. Chandra, A.N. Sahay, S.M. Mobin and D.S. Pandey, J. Organomet. Chem. 658, 43 (2002) http://dx.doi.org/10.1016/S0022-328X(02)01598-X10.1016/S0022-328X(02)01598-XSearch in Google Scholar

[8] Z. Xu, S. White, L.K. Thompson, D.O. Miller, M. Ohba, H. Kawa, C. Wilson and J.A.K. Howard, J. Chem. Soc., Dalton Trans. 1751 (2000) 10.1039/a909824kSearch in Google Scholar

[9] S. Pal and S. Pal, Inorg. Chem. 40, 4807 (2001) http://dx.doi.org/10.1021/ic010310y10.1021/ic010310ySearch in Google Scholar PubMed

[10] D.R. McMillin and K.M. McNett, Chem. Rev. 98, 1201 (1998) http://dx.doi.org/10.1021/cr960116710.1021/cr9601167Search in Google Scholar PubMed

[11] Z. Mao, H.-Y. Chao, Z. Hui, C.-M. Che, W.-F. Fu, K.-K. Cheung and N.Y. Zhu, Chem. Eur. J. 9, 2885 (2003) http://dx.doi.org/10.1002/chem.20020461010.1002/chem.200204610Search in Google Scholar

[12] S. Hu, J.-C. Chen, M.-L. Tong, B. Wang, Y.-X. Yan, and S.R. Batten, Angew. Chem. Int. Ed. 44, 5471 (2005) http://dx.doi.org/10.1002/anie.20050175310.1002/anie.200501753Search in Google Scholar

[13] Y.-C. Liu, C.-I. Li, W.-Y. Yeh, G.-H. Lee and S.-M. Peng, Inorg. Chim. Acta 359, 2361 (2006) http://dx.doi.org/10.1016/j.ica.2006.02.03810.1016/j.ica.2006.02.038Search in Google Scholar

[14] W.-F. Fu, X. Gan, J. Jiao, Y. Chen, M. Yuan, S.-M. Chi, M.-M. Yu and S.-X. Xiong, Inorg. Chim. Acta 360, 2758 (2007) http://dx.doi.org/10.1016/j.ica.2007.02.00710.1016/j.ica.2007.02.007Search in Google Scholar

[15] Q.-Y. Cao, X. Gan, W.-F. Fu, Z. Anorg. Allg. Chem. 633, 176 (2007) http://dx.doi.org/10.1002/zaac.20060019610.1002/zaac.200600196Search in Google Scholar

[16] Y.-M. Wang, F. Teng, Y.-B. Hou, Z. Xu, and Y.-S. Wang, Appl. Phys. Lett. 87, 233512 (2005) http://dx.doi.org/10.1063/1.213998710.1063/1.2139987Search in Google Scholar

[17] Z. Mao, J.-S. Huang, C.-M. Che, N.Y. Zhu, S.K.-Y. Leung, and Z.-Y. Zhou, J. Am. Chem. Soc. 127, 4562 (2005) http://dx.doi.org/10.1021/ja042335c10.1021/ja042335cSearch in Google Scholar

[18] C.-M. Che, Z. Mao, V.M. Miskowski, M.-C. Tse, C.-K. Chan, K.-K. Cheung, D.L. Phillips and K.-H. Leung, Angew. Chem., Int. Ed. 39, 4084 (2000) http://dx.doi.org/10.1002/1521-3773(20001117)39:22<4084::AID-ANIE4084>3.0.CO;2-N10.1002/1521-3773(20001117)39:22<4084::AID-ANIE4084>3.0.CO;2-NSearch in Google Scholar

[19] W.-F. Fu, X. Gan, C.-M. Che, Q.-Y. Cao, Z.-Y. Zhou and N. N.-Y. Zhu, Chem. Eur. J. 10, 2228 (2004) http://dx.doi.org/10.1002/chem.20030565710.1002/chem.200305657Search in Google Scholar

[20] G.J. Kubas, B. Monzyk and A.L. Crumbliss, Inorg. Synth. 19, 90 (1979) http://dx.doi.org/10.1002/9780470132500.ch1810.1002/9780470132500.ch18Search in Google Scholar

[21] G.M. Sheldrick, SHELXS-97: Program for the Solution of Crystal Structures, University of Gottingen (Gottingen, Germany, 1997) Search in Google Scholar

[22] Z.-F. Yao: “Synthesis, characterization and photochemical nature research of novel controllable ATRP catalysts”, Ph. M. Dissertation, Yun Nan Normal University (Kunming, China, 2004). Search in Google Scholar

[23] M.-M. Yu, W.-F. Fu, Z.-X. Li, Z.-F. Yao and L.-F. Jia, Acta Cryst. E60, m1897 (2004) Search in Google Scholar

Published Online: 2008-10-28
Published in Print: 2008-12-1

© 2008 Versita Warsaw

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