Table 13C NMR chemical shifts of phenylacetylides

Acetylides
solvent
δCi (ppm)
Ph-C≡C-M
δCt (ppm)
Ph-C≡C-M
ref.
Ph-C≡C-Li
THF
n.r.
139.35
1
Ph-C≡C-Al
CDCl3
107.5
101.2
2
Ph-C≡C-Ga
CDCl3
107.2
99.2
2
Ph-C≡C-Fe
DMSO-d6
119.0
108.7
3
Ph-C≡C-Fe
solvent
132.4 - 132.7
145.4 - 147.6
4
Ph-C≡C-Ru
CD2Cl2
110.9
107.6
5
Ph-C≡C-Re
solvent
114.8 - 118.7
105.9 - 117.1
6
(MeO)Ph-C≡C-Fe
solvent
119.5
136.8
4
(Me)Ph-C≡C-Ru
CD2Cl2
109.5
108.0
5
(HC≡C)Ph-C≡C-Re
solvent
113.9 - 118.8
107.1 - 123.3
6
  1. T. F. Briggs, M. D. Winemiller, D. B. Collum, R. L. Parsons, Jr., A. H. Davulcu, G. D. Harris, J. M. Fortunak, P. N. Confalone, J. Am. Chem. Soc. 2004, 126, 5427-5435.
  2. M. Schiefer, N. D. Reddy, H. J. Ahn, A. Stasch, H. W. Roesky, A. C. Schlicker, H. G. Schmidt, M. Noltemeyer, D. Vidovic Inorg. Chem. 2003, 42, 4970.
  3. G. Albertin, P. Agnoletto, S. Antoniutti Polyhedron 2002, 21, 1755.
  4. L. D. Field, A. J. Turnbull, P. Turner J. Am. Chem. Soc. 2002, 124, 3692.
  5. G. Albertin, S. Antoniutti, E. Bordignon, M. Granzotto J. Organomet. Chem. 1999, 585, 83.
  6. G. Albertin, S. Antoniutti, E. Bordignon, D. Bresolin J. Organomet. Chem. 2000, 609, 10.