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Synthesis of Functionalized Tris(2-propoxyphenyl)phosphine Oxides as Precursors of Tripodal Propeller-Shaped Ligands

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Abstract

A series of precursors of novel tripodal ligands (2-XCH2CH2CH2OC6H4)3PO, where X = AcO, HO, MeSO2O, Br, N3, were synthesized by the alkylation of the starting tris(2-hydroxyphenyl)phosphine oxide with 3-bromopropyl acetate followed by hydrolysis of the resulting triacetate to triol and conversion of the latter to trimesylate. Treratment of the resulting trimesylate with LiBr or NaN3 was used to prepare the corresponding tribromo or triazido derivatives.

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References

  1. Sartain, H.T., McGraw, S.N., Lawrence, C.L., Werner, E.J., and Biros, S.M., Inorg. Chim. Acta, 2015, vol. 426, p. 126. doi 10.1016/j.ica.2014.11.032

    Article  CAS  Google Scholar 

  2. Thammavongsy, Z., Khosrowabadi Kotyk, J.F., Tsay, C., and Yang, J.Y., Inorg. Chem., 2015, vol. 54, no. 23, p. 11505. doi 10.1021/acs.inorgchem.5b02133

    Article  CAS  PubMed  Google Scholar 

  3. Khansari, M.E., Johnson, C.R., Basaran, I., Nafis, A., Wang, J., Leszczynski, J., and Hossain, Md.A., RSC Adv., 2015, vol. 5, no. 23, p.17606. doi 10.1039/C5RA01315A

  4. Beletskiy, E.V., Wang Xue-Bin, and Kass, S.R., J. Phys. Chem. A, 2016, vol. 120, no. 42, p. 8309. doi 10.1021/acs.jpca.6b08438

    Article  CAS  PubMed  Google Scholar 

  5. Mazik, M., Chem. Soc. Rev., 2009, vol. 38, no. 4, p. 935. doi 10.1039/b710910p

    Article  CAS  PubMed  Google Scholar 

  6. Mazik, M. and Cavga, H., J. Org. Chem., 2006, vol. 71, no. 8, p. 2957. doi 10.1021/jo052479p

    Article  CAS  PubMed  Google Scholar 

  7. Rachuri, Y., Bisht, K. K., and Suresh, E., Cryst. Growth Des., 2014, vol. 14, no. 7, p. 3300. doi 10.1021/cg500188n

    Article  CAS  Google Scholar 

  8. Oishil, M., Ichinose, Y., and Nomura, N., Eur. J. Inorg. Chem., 2016, no. 10, p. 1596. doi 10.1002/ejic.201501438

    Article  CAS  Google Scholar 

  9. Zhang, M., Liang, Z., Ling, J., Ni, X., and Shen, Z., Dalton Trans., 2015, vol. 44, no. 24, p. 11182. doi 10.1039/c5dt01241d

    Article  CAS  PubMed  Google Scholar 

  10. Guillet G.L., Hyatt, I.F.D., Hillesheim, P.C., Abboud, K.A., and Scott, M.J., New J. Chem., 2013, vol. 37, no. 1, p. 119. doi 10.1039/c2nj40586e

    Article  CAS  Google Scholar 

  11. Konishi, A., Nakajima, H., Maruyama, H., Yoshioka, S., Baba, A., and Yasuda, M., Polyhedron, 2017, vol. 125, p. 130. doi 10.1016/j.poly.2016.10.019

    Article  CAS  Google Scholar 

  12. Paraskevopoulou, P., Wang, L. Ai, Q., Pinnapareddy, D., Acharyya, R., Dinda, R., Das, P., Celenligil-Cetin, R., Floros, G., Sanakis, Y., Choudhury, A., Rath, N.P., and Stavropoulos, P., Inorg. Chem., 2010, vol. 49, no. 1, p. 108. doi 10.1021/ic9015838

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Jones, M.B., Hardcastle, K.I., Hagen, K.S., and Mac-Beth, C.E., Inorg. Chem., 2011, vol. 50, no. 14, p. 6402. doi 10.1021/ic2007183

    Article  CAS  PubMed  Google Scholar 

  14. Chu, L., Hardcastle, K. I., and MacBeth, C. E., Inorg. Chem., 2010, vol. 49, no. 16, p. 7521. doi 10.1021/ic1008347

    Article  CAS  PubMed  Google Scholar 

  15. Matloka, K., Gelis, A., Regalbuto, M., Vandegrift, G., and Scott, M.J., Sep. Sci. Technol., 2006, vol. 41, no. 10. p. 2129. doi 10.1080/01496390600745727

  16. Kudryavtsev, I.Yu., Baulina, T.V., Pasechnik, M.P., Aisin, R.R., Matveev, S.V., Petrovskii, P.V., and Nifant’ev, E.E., Russ. Chem. Bull., 2013, vol. 62, no. 4, p. 1086. doi 10.1007/s11172-013-0146-6

    Article  CAS  Google Scholar 

  17. Kudryavtsev, I.Yu., Baulina, T.V., Pasechnik, M.P., Matveev, S.V., and Matveeva, A.G., Phosphorus, Sulfur, Silicon, Relat. Elem., 2014, vol. 189, p. 946. doi 10.1080/10426507.2014.904865

    Article  CAS  Google Scholar 

  18. Matveeva, A.G., Kudryavtsev, I.Yu., Pasechnik, M.P., Vologzhanina, A.V., Baulina, T.V., Vavina, A.V., Sukat, G.Ya., Matveev, S.V., Godovikov, I.A., Turanov, A.N., Karandashev, V.K., and Brel, V.K., Polyhedron, 2018, vol. 142, p. 71. doi 10.1016/j.poly.2017.12.025

    Article  CAS  Google Scholar 

  19. Kudryavtsev, I.Yu., Baulina, T.V., Khrustalev, V.N., Petrovskii, P.V., Pasechnik, M.P., and Nifant’ev, E.E., Dokl. Chem., 2013, vol. 448, no. 2, p. 55. doi 10.1134/S0012500813020092

    Article  CAS  Google Scholar 

  20. Armarego, W.L.F. and Chai, C.L.L., Purification of Laboratory Chemicals, Amsterdam: Elsevier, 2009. doi 10.1134/S0044460X1809024X

    Google Scholar 

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Correspondence to Т. V. Baulina.

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Dedicated to the 110th anniversary of M.I. Kabachnik’s birth

Original Russian Text © Т.V. Baulina, I.Yu. Kudryavtsev, G.Ya. Sykat, V.K. Brel’, 2018, published in Zhurnal Obshchei Khimii, 2018, Vol. 88, No. 9, pp. 1559–1562.

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Baulina, Т.V., Kudryavtsev, I.Y., Sykat, G.Y. et al. Synthesis of Functionalized Tris(2-propoxyphenyl)phosphine Oxides as Precursors of Tripodal Propeller-Shaped Ligands. Russ J Gen Chem 88, 1927–1930 (2018). https://doi.org/10.1134/S1070363218090281

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