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活泼氢本身化学位移值就是有一个较大的变动范围吧。
P0 D& c* H6 l9 H8 i7 e0 \0 s1 w至于积分值，一般要比按化合物的分子式算出来的比例要小。
/ J, V0 J* {) }' t6 W原因很多，H交换是一个，积分基线也是一个。前段时间看Simpson的Organic Structure Determination
Using 2-D NMR Spectroscopy，里面有提到： ) ?0 i: s0 O2 \) l* V% C4 q
0 ^7 p8 Y2 T0 F9 o, Y
There are several possible reasons to account for why we observe the
low integral values for 1H’s bound to heteroatoms despite having a
sufficiently long relaxation delay between scans. First, relaxation (T 2 )
may occur to a greater extent for those 1H’s whose signals are broad as
a result of the time delay between the read pulse and the start of the
digitization of the FID. Because a broad resonance in the frequency
domain corresponds to a rapidly decaying signal amplitude in the
time domain, broad resonances will often generate low integrals. A
second possible reason for a low integral value is that baseline correction
of the spectrum may wipe out the edges of broad resonances,
thus subtracting intensity from the peak. A third possible reason for
a low integral value of a 1H on a heteroatom may result from partial
chemical exchange of these 1H’s with deuterons ( 2H’s) in the solvent,
especially if the solvent is deuterated water or methanol
/ m9 d+ Z5 B: y P: ][此贴子已经被作者于2009-10-28 19:00:43编辑过] $ X) K1 k6 b" G& S' e
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发表于 2008-11-20 15:17:21
发表于 2008-11-20 15:46:39
