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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。
" R- z- y. I4 ~; }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。
9 o x6 A, n% h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： $ G U" ~! X, Y7 s/ i, G& S8 a
5 p% I1 a8 }3 J: t% Z( A1 F6 C
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
5 l" K7 w2 d7 H6 _, m7 {[此贴子已经被作者于2009-10-28 19:00:43编辑过]
6 X H' X) \+ w+ e- a( t% L7 b | 
发表于 2008-11-20 15:17:21
发表于 2008-11-20 15:46:39
