Chemical Shift Table

For certain compounds, the listed chemical shift pertains to the F shown in bold. The primary references for these values are:
1) the 1991 Bruker Almanac, and
2) Compilation of reported F19 NMR chemical shifts, 1951 to mid-1967 by Claude H. Dungan and John R. Van Wazer.
Negative shifts are those that appear upfield of CFCl3 and positive shifts are those that appear downfield.
Compound Chemical Shift (ppm)
Relative to neat CFCl3
CFCl3 0.00
MeF -271.9
CF3H (in CFCl3) -78.6
CF3H (in EtO) -78.6
CF2H2 -143.6
EtF -213
FCH=CH2 -114
F2C=CH2 -81.3
F2C=CF2 -135
CF3COOH (in CFCl3) -76.55
CF3COOH (neat) -78.5
CF3COOH (in CCl4 -76.3
CF3COOC6H6 -73.85
CF3COOCH2C6H6 -75.02
CF3COOCH3 -74.21
CF3COOEt (neat) -78.7
CF3COO(CH2)n -74 to -75
C6F6 -164.9
C6H5F -113.5
p-FC6H4F -106.0
CFH2Ph -207
C6H5CF3 -63.72
C4F8 -135.15
C5F10 -132.9
CF3R -60 to -70
CHF2OR ~-82
(CF3)2CO -84.6
CH2CN -251
F2 +422.92
CF3Cl -28.6
ClF3 +116, -4
ClF5 +247,+412
CF2Cl2 -8
CFCl2CFCl2 -67.8
CFBr3 +7.38
CF2Br2 +7
IF4F(equatorial) +58.9
IF7 +170
AsF3 -40.6
AsF5 -66
[AsF6]-1 -69.5
BF3 -131.3
(CH3)2O.BF3 -158.3
(C2H5)2O.BF3 -153
[BeF4]-1 -163
MoF6 -278
ReF7 +345
SF6 +57.42
SO2F -78.5
S2O5F2 +47.2
SbF5 -108
[SbF6]-1 -109
SeF6 +55
(C2H5)2SiF2 -143.0
SiF4 -163.3
[SiF6]-2 -127
TeF6 -57
WF6 +166
XeF2 +258
XeF4 +438
XeF6 +550
NF3 147
SOF2 75.68
C6H5SO2F (dilute) 65.464
C6H5SO2F (20% conc)65.514
SF6 (dilute) 57.617
SF6 (10% conc 57.42
SO2F2 33.17
CBr3F (dilute) 7.388
CBr3F (80% conc) 7.043
CCl2F2 -6.848
CClF3 -28.1
PF3 -34.0
(CF3)3N (dilute) -55.969
(CF3)3N (30% conc) -55.969
CF3CF2CF2I -60.470
CF4 -62.3
C6H5CF3 (dilute) -63.732
C6H5CF3 (40% conc) -63.370
PF5 -71.5
CCl2F.CCl2F (dilute)-67.775
CCl2F.CCl2F (20% conc)-67.834
(CF3)3CF -74.625
CF3CO2H (dilute) -76.530
CF3CO2H (20% conc) -76.542
CF3(CF2)5CF3-81.60
CF3(CF2)2CF3-81.85
[CF3CF2CF2]N-85.19
POF3 -90.7
CF3CF2CF2CF2CN-107.1
CF3CF2CF2CF2CN-105.764

Homonuclear Couplings

Listed Coupling constant values pertain to Fs shown in bold.
Compound Coupling Constant (Hz)
(CF3CF2)2NCF3 10.2
(CF3CF2)2NCF3 15.18
(CF3CF2)2NCF3 6.8
[CF3CF2]3N 13.6
CF3CF2N[CF3]2 <1
CF3CF2N[CF3]2 16
CF3CF2N[CF3]2 6
(CF3CF2)2O 3.4
(CF3]3CF 1.4
CF3CF2H 2.8
CF3CFH2 15.5
CF3CF2CHF2 4.5
CF3CF2CHF2 7.3
CF3CF2CH2F 15.2
CF3CF2CH2F 7.9
CF2Cl.CF2.CH2F 15.1
CF2Cl.CF2.CH2F 7.7
CF2Cl.CF2.CH2F 3.9
CF2Br.CF2.CH2F 15.5
CF2Br.CF2.CH2F 7.7
CF2Br.CF2.CH2F 3.9
CFFBr.CHFBr 21
CFFBr.CHFBr 24
CFFBr.CHFBr 174
CFFBr.CHFCl 18
CFFBr.CHFCl 18
CFFBr.CHFCl 177
CFFBr.CFClBr 13
CFFBr.CFClBr 14
CFFBr.CFClBr 159
CFF(SiCl3).CFClBr 16.8
CFF(SiCl3).CFClBr 16.8
CFF(SiCl3).CFClBr 343
CF3.CFF.CFICl 270.4
CFF=CFCl 76
CFF=CFCl (cis) 56
CFF=CFCl (trans) 116
CFCl=CFCl (cis) 37.5
CFCl=CFCl (trans) 129.57
CFF=CFCF3 57
CFF=CFCF3 (cis) 39
CFF=CFCF3 (trans) 116
CFF=CFCF3 (trans) 8
CFF=CFCF3 (cis) 22
CFF=CFCF3 13
(cyclopropane) CH2.CFF.CHCH3 157
(cyclobutane) CH2.CFF.CCl2.CCl2187
(cyclobutene) CFF.CH(C2H5).CCl2=CCl 192
(cyclobutane) CFF.CFF.CH2.CHCClH2 230
(cyclobutane) CFF.CFF.CH2.CHCClH2 240
(cyclohexane) CFH.CFH.CFH.CFH.CFH.CFF 284