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1
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0003487210
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0037116525
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Dorta, R.1
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Milstein, D.4
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14
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0030797978
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(a) Cooper, A. C.; Streib, W. E.; Eisenstein, O.; Caulton, K. G. J. Am. Chem. Soc. 1997, 119, 9069.
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16
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(c) Cooper, A. C.; Clot, E.; Huffman, J. C.; Streib, W. E.; Maseras, F.; Eisenstein, O.; Caulton, K. G. J. Am. Chem. Soc. 1999, 121, 97.
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Caulton, K.G.7
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19
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0038536214
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note
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A closely related aryl-iridium complex was reported recently.
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20
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0038197523
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note
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Strictly anhydrous solvents have to be used for the synthesis of compound 1.
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21
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0034683151
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The X-ray crystal structure of the rhodium compound has been determined; see: Werner, H.; Schneider, M. E.; Bosch, M.; Wolf, J.; Teuben, J. H.; Meetsma, A.; Troyanov, S. I. Chem. Eur. J. 2000, 6, 3052.
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(2000)
Chem. Eur. J.
, vol.6
, pp. 3052
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Werner, H.1
Schneider, M.E.2
Bosch, M.3
Wolf, J.4
Teuben, J.H.5
Meetsma, A.6
Troyanov, S.I.7
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22
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0037859753
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note
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Attempts to precipitate 2 were not successful, due to what appeared to be substitution of the COE ligands by the excess acetontrile present during workup. Unfortunately, weakly coordinating solvents (such as chloroform, dichloromethane, nitromethane, and benzene) reacted with complex 1 and excluded the use of stoichiometric amounts of acetonitrile for the synthesis of complex 2.
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23
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0038197483
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note
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Attempts to observe and isolate intermediates prior to C-H activation did not succeed.
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24
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0037522191
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note
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2 signal confirms the trans configuration of the phosphines in complex 4.
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25
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0037522181
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(a) Hietkamp, S.; Stufkens, D. J.; Vrieze, K. J. Organomet. Chem. 1977, 139, 189.
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J. Organomet. Chem.
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Hietkamp, S.1
Stufkens, D.J.2
Vrieze, K.3
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27
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0038536166
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note
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3P was not selective and led to a mixture of products.
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31
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0037522183
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note
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2)]}, shows resonances at δ 19.6 and 62.2 ppm.
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33
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37049136806
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(b) Masters, C. J.; Shaw, B. L.; Stainbank, R. E. J. Chem. Soc., Chem. Commun. 1971, 209.
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(1971)
J. Chem. Soc., Chem. Commun.
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Masters, C.J.1
Shaw, B.L.2
Stainbank, R.E.3
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34
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0001394070
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(c) Cooper, A. C.; Huffman, J. C.; Caulton, K. G. Organometallics 1997, 16, 1974.
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(1997)
Organometallics
, vol.16
, pp. 1974
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Cooper, A.C.1
Huffman, J.C.2
Caulton, K.G.3
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35
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0034623550
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(d) Kanzelberger M.; Singh, B.; Czerw, M.; Krogh-Jespersen, K.; Goldman, A. S. J. Am. Chem. Soc. 2000, 122, 11017.
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(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 11017
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Kanzelberger, M.1
Singh, B.2
Czerw, M.3
Krogh-Jespersen, K.4
Goldman, A.S.5
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36
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0037859748
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note
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6 solution), and data from these crystals were measured. The symmetry of the crystals (I4/m or R3̄) and the location of the Ir on special positions meant that the structure of 6 could not be refined satisfactorily (cf. ref 6c); however, the absence of coordinated solvent molecules could be clearly seen.
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