Table
13
C NMR chemical shifts of phenylacetylides
Acetylides
solvent
δ
C
i
(ppm)
Ph-
C
≡C-M
δ
C
t
(ppm)
Ph-C≡
C
-M
ref.
Ph-C≡C-Li
THF
n.r.
139.35
1
Ph-C≡C-Al
CDCl
3
107.5
101.2
2
Ph-C≡C-Ga
CDCl
3
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
CD
2
Cl
2
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
CD
2
Cl
2
109.5
108.0
5
(HC≡C)Ph-C≡C-Re
solvent
113.9 - 118.8
107.1 - 123.3
6
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.
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.
G. Albertin, P. Agnoletto, S. Antoniutti
Polyhedron
2002
,
21
, 1755.
L. D. Field, A. J. Turnbull, P. Turner
J. Am. Chem. Soc.
2002
,
124
, 3692.
G. Albertin, S. Antoniutti, E. Bordignon, M. Granzotto
J. Organomet. Chem.
1999
,
585
, 83.
G. Albertin, S. Antoniutti, E. Bordignon, D. Bresolin
J. Organomet. Chem.
2000
,
609
, 10.