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[求助]伯胺谱图解析问题

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发表于 2009-10-28 11:45:51 | 显示全部楼层

活泼氢本身化学位移值就是有一个较大的变动范围吧。

8 V6 d8 m+ O8 z3 h

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。

3 l3 Z, [# b6 o# D' i8 o

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:

6 Y& F5 z! H+ p

 

U8 z# \9 L. g! o3 Y7 U

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 ~ V& @% {% C: ]8 J4 K5 A- t
[此贴子已经被作者于2009-10-28 19:00:43编辑过]
- ]4 ]: X9 c+ ~) }" b
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发表于 2009-11-8 22:48:19 | 显示全部楼层
学习了
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发表于 2009-11-11 13:40:06 | 显示全部楼层
这可以从N原子上H的交换速度和N的电四极矩弛豫进行考虑。
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