VINYLLITHIUM - DYNAMIC BEHAVIOR IN TETRAHYDROFURAN SOLUTION AND COMPREHENSIVE ANALYSIS OF NMR SPIN-SPIN COUPLING-CONSTANTS

被引:47
作者
BAUER, W [1 ]
GRIESINGER, C [1 ]
机构
[1] JOHANN WOLFGANG GOETHE UNIV,INST ORGAN CHEM,D-60439 FRANKFURT,GERMANY
关键词
D O I
10.1021/ja00076a051
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Vinyllithium (ViLi; isotopically labeled with Li-6) is an 8:1 tetramer/dimer equilibrium in tetrahydrofuran-d8 (THF-d8) at -90-degrees-C (1.6 M solution). In the presence of equilmolar amounts of TMEDA (tetramethylethylenediamine), the tetramer:dimer ratio is 1:13 in THF-d8 at -80-degrees-C (1.9 M solution). Dynamic NMR phenomena are observed in the ViLi tetramer: at -90-degrees-C in THF-d8, a ''static'' aggregate is found, whereas at -60 -degrees-C rapid intraaggregate exchange of the four lithium sites indicates a ''fluxional'' tetramer. Within a ''static'' tetramer, rapid tumbling of a monomer unit is deduced from C, Li and H, Li NMR coupling patterns. From tilts within cross peak multiplets in H-1, C-13 HETCOR spectra of ViLi (due to coupling with the passive Li-6 spin), it is concluded that the sign of 1J(C-13, Li-6) is positive. In a fully coupled heteronuclear Li-6, H-1 shift correlation experiment (FUCOUP), an intense and a weaker cross peak are observed between Li-6, H(gem) and Li-6, H(trans), respectively, of tetrameric ViLi. This is indicative of scalar Li-6, H-1 coupling. In a Li-6, H-1 FUCOUP spectrum with a small (36-degrees) H-1 mixing pulse (''beta-FUCOUP''), the tilt of the Li-6, H(trans) cross peak indicates the sign and magnitude of 2J(Li-6, H(gem)) to be +0.4Hz. Analogous to the tetramer, Li-6, H-1 beta-FUCOUP of the dimer reveals 3J(Li-6, H(trans)) to be +0.4 Hz. The C-13, C-13 coupling constant in vinyllithium is extraordinarily small (dimer, 35.0 Hz; tetramer, 36.3 Hz). Likewise,the one-bond C-13, H-1 coupling constant 1J(C1, H(gem)) is the lowest reported so far for monosubstituted ethylenes (dimer, 91.7 Hz; tetramer, 93.2 Hz). By combination of C-13 gated decoupled and C-13, H-1 beta-FUCOUP data, extreme numbers are also found for geminal 2J(C-13, H-1) coupling constants: dimer, 2J(C1, H(cis)) = +13.5 HZ; 2J(C1, H(trans) = -5.9 Hz; 2J(C2, H(gem)) = -10.5 Hz; tetramer, 2J(C1, H(cis)) = +13.5 HZ; 2J(C1, H(trans)) = -6.1 HZ; 2J(C2,H(gem)) = -12.1 Hz.
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页码:10871 / 10882
页数:12
相关论文
共 104 条
[1]  
Abraham R.J., 1971, ANAL HIGH RESOLUTION
[2]  
Akitt J.W., 1987, MULTINUCLEAR NMR
[3]   STRUCTURAL NMR INVESTIGATIONS ON ALLYLLITHIUM COMPOUNDS [J].
BALZER, H ;
BERGER, S .
CHEMISCHE BERICHTE-RECUEIL, 1992, 125 (03) :733-737
[4]  
BANWELL CN, 1962, DISCUSS FARADAY SOC, V34, P115
[5]  
BANWELL CN, 1960, SPECTROCHIM ACTA, V11, P794
[6]   STUDIES OF C-13-C-13 COUPLING-CONSTANTS .4. ISOPROPENYL SYSTEM [J].
BARTUSKA, VJ ;
MACIEL, GE .
JOURNAL OF MAGNETIC RESONANCE, 1972, 7 (01) :36-&
[7]   MECHANISTIC EVIDENCE FOR ORTHO-DIRECTED LITHIATIONS FROM ONE-DIMENSIONAL AND TWO-DIMENSIONAL NMR-SPECTROSCOPY AND MNDO CALCULATIONS [J].
BAUER, W ;
SCHLEYER, PV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (18) :7191-7198
[8]   THE MECHANISM OF DIRECTED 2ND LITHIATIONS - DETECTION OF SHORT PROTON-LITHIUM SEPARATIONS BY 6LI-1H HOESY [J].
BAUER, W ;
CLARK, T ;
SCHLEYER, PV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (04) :970-977
[9]   STRUCTURE OF A SUPER BASE IN TETRAHYDROFURAN SOLUTION STUDIED BY LI-6, H-1 HOESY, CS-133, H-1 HOESY, AND MNDO - EVIDENCE FOR DISCRETE SPECIES RATHER THAN A MIXED AGGREGATE [J].
BAUER, W ;
LOCHMANN, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (19) :7482-7489