[求助]伯胺谱图解析问题

louluv

活泼氢本身化学位移值就是有一个较大的变动范围吧。

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。

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：

. r6 ~/ X* Q7 x7 V9 }' C8 B

 

0 M) z, I* W3 R; B7 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

[此贴子已经被作者于2009-10-28 19:00:43编辑过]

/ x2 F0 a+ U n

coki2008xmu

学习了

levona

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。