SYNTHESIS OF NEW ORGANODERIVATIVES OF LOWER LANTHANIDES

References

• Wilkinson , G. and Birmingham , J. M. 1954 . J. Am. Chem. Soc. , 76 : 6210
   Web of Science ®Google Scholar
• Birmingham , J. M. and Wilkinson , G. 1956 . J. Am. Chem. Soc. , 78 : 42 – 44 .
   Web of Science ®Google Scholar
• Maginn , R. E. , Manastyrskyj , S. and Dubeek , M. 1963 . J. Am. Chem. Soc. , 85 : 672 – 676 .
   Web of Science ®Google Scholar
• Manastryskyj , S. , Maginn , R. E. and Dubeek , M. 1963 . Inorg. Chem. , 2 : 904 – 905 .
   Web of Science ®Google Scholar
• Manastyrskyj , S. and Dubeek , M. 1964 . ibid. , 3 : 1674 – 1648 .
   Google Scholar
• Fischer , E. 0. and Fischer , H. 1965 . J. Orgunomet. Chem. , 3 : 181 – 187 .
   Google Scholar
• Tsutsui , M. , Tankino , T. and Lorenz , D. 1966 . Z. Nafurforsch. , 21 : 1 – 2 .
   Google Scholar
• Watt , G. W. and Gillow , E. W. 1969 . J. Am. Chem. Soc. , 91 : 115 – 776 .
   Google Scholar
• Hayes , R. G. and Thomas , J. L. 1969 . J. Am. Chem. Soc. , 91 : 6876
   Google Scholar
• Hodgson , K. A. , Mares , F. , Starks , D. F. and Streitwieser, Jr. , A. 1973 . J. Am. Chem. Soc. , 95 : 8050 – 8658 .
   Google Scholar
• Ely , S. R. , Hopkins , T. E. and Dekock , C. W. 1976 . J. Am. Chem. Soc. , 98 : 1624 – 1625 .
   Web of Science ®Google Scholar
• Tsutsui , M. and Gysling , H. J. 1969 . J. Am. Chem. Soc. , 91 : 3175 – 3178 .
   Web of Science ®Google Scholar
• Schumann , H. and Hohmann , S. 1976 . Chem.-Ztg. , 100 : 336
   Google Scholar
• Evans , W. J. , Engerer , S. C. and Neville , S. C. 1978 . J. Am. Chem. Soc. , 100 : 331 – 333 .
   Web of Science ®Google Scholar
• Cotton , S. A. , Hart , F. A. , Hursthouse , B. M. and Welch , A. J. 1972 . J. Chem. Soc. Chem. Comm. , : 1225 – 1226 .
   Google Scholar
• Tsutsui , M. and Ely , N. 1974 . J. Am. Chem. Soc. , 96 : 4042 – 4043 .
   Web of Science ®Google Scholar
• Tsutsui , M. and Ely , N. 1975 . J. Am. Chein. Soc. , 97 : 1280 – 1281 .
   Web of Science ®Google Scholar
• Tsutsui , M. and Ely , N. 1975 . J. Am. Chem. Soc. , 97 : 3551 – 3553 .
   Web of Science ®Google Scholar
• Ely , N. M. and Tsutsui , M. 1975 . Inorg. Chem. , : 2680 – 2687 .
   Web of Science ®Google Scholar
• Schumann , H. and Miiller , J. 1978 . J. Organomet. Chem. , 146 : C5 – C7 .
   Web of Science ®Google Scholar
• Deacon , G. B. and Koplick , A. 1978 . J. Organomet. Chem. , 144 : C43 – C45 .
   Web of Science ®Google Scholar
• Schumann , H. and Cygon , M. 1978 . Organomet. Chem. , 144 : C43 – C45 .
   Web of Science ®Google Scholar
• Wayda , A. L. and Evans , W. J. 1978 . J. Am. Chem. Soc. , 100 : 7119 – 7121 .
   Web of Science ®Google Scholar
• Hillman , M. and Weiss , A. J. 1972 . J. Organomet. Chem. , 42 : 123 – 128 .
   Web of Science ®Google Scholar
• Prepared from the reaction of ardium metal and elbynyl benzene in ethyl ether
   Google Scholar
• Elemental analyses were preformed by Schwarzkopf Microanalytical Laboratories, Woodside, N.Y. Anal. Calcd. (chloride) for C, HI, LaCI: C, 45.3; H, 4.11; La,40.31;CI, 10.28. Found:C,43S;H. 5.13; La, 39.67;C1, 10.31. Calcd. for C, H, CeCI: C, 45.15; H,4.08;Ce,40.52;Cl, 10.25. Found: C, 43.5;H, 5.16; Ce 39.18; C110.74. Calcd. [phenyl ethynyl) for C, H, La: La, 33.85. Found: 35.66. Calcd. for C, H, Ce: Ce, 34.05. Found: 34.71
   Google Scholar
• For example [1,1′(CH2)3 (η5-Ca H412 1 La[sbnd]M[dbnd]C, H5: Ir (Nujol, cm−1) 3080 (9 2934 (s), 2867 (9, 2052 (s), 1061 (br), 1045 (s), 1024 (m), 1003 (m), 945 (m), 857 (m), 760 (s), 668 (s)
   Google Scholar
• King , C. W. and So , S. P. 1970 . J. Mol Specrros. , 36 : 468 – 487 .
   Web of Science ®Google Scholar
• Cotton , F. A. and Marks , T. J. 1969 . J. Am. Chem. Soc. , 91 : 7281 – 7285 .
   Web of Science ®Google Scholar
• Van Vleck , J. H. and Frank , N. 1929 . Phys. Rev. , 34 : 1494 – 1496 .
   Google Scholar
• Mares , F. , Hodgson , K. 0. and Streitureser, Jr. , A. 1971 . J. Organomet. Chem. , 28 : C24 – C26 .
   Web of Science ®Google Scholar
• Cockerill , A. F. , Davies , G. L. 0. , Harden , R. C. and Rackham , D. M. 1973 . Chem. Rev. , 73 : 553 – 588 .
   Web of Science ®Google Scholar
• NMR data in ppm is based on upfield THF peak occurring at δ = 1.79
   Google Scholar