|
活泼氢本身化学位移值就是有一个较大的变动范围吧。
+ m: O: Q+ B, o& I3 S* K8 V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; v9 L7 E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： 2 L& P: f6 A' h. X2 y0 X
5 T6 w! ]4 U% F9 b' X- G
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 & q/ O# i3 h! S" J+ W+ W# {1 e
[此贴子已经被作者于2009-10-28 19:00:43编辑过]
0 u& g+ H0 x1 [* {6 p' Q | 
发表于 2008-11-20 15:17:21
发表于 2008-11-20 15:46:39
