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如何学习核磁共振?听北冥给你讲讲。

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发表于 2009-9-24 16:57:52 | 显示全部楼层
北冥有鱼,其实你可以自已这编一本有质量有系统的书啊!!!!!!
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发表于 2009-9-28 23:51:38 | 显示全部楼层
谢谢了
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发表于 2009-10-1 14:38:14 | 显示全部楼层
整个帖子看下来,不得不佩服北冥老师的核磁方面的知识,这个帖子真的值得慢慢看,多次看,慢慢消化。
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发表于 2009-10-2 01:36:46 | 显示全部楼层
 thankssssssssssss
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发表于 2009-10-6 18:43:59 | 显示全部楼层
说的没错,呵呵
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发表于 2009-10-18 13:18:27 | 显示全部楼层

好强大啊..

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发表于 2009-10-18 20:29:13 | 显示全部楼层
我现在也刚刚在学习如何解析核磁谱图,想问一下谱图峰强度低是怎么回事啊!
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发表于 2009-10-20 23:02:35 | 显示全部楼层
 介绍一本新书 Classics in Spectroscopy (2009)



 

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发表于 2009-10-20 23:05:50 | 显示全部楼层
http://www.wiley.com/WileyCDA/WileyTitle/productCd-3527325166,descCd-authorInfo.html

Description:
Classics in Spectroscopy: Isolation and Structure Elucidation of Natural Products
) P( V: F) w1 d, o+ his the first book of its kind to describe the art of NMR using everyday- M8 a* c+ [6 j9 I, u6 w examples. This textbook will not only fascinate students wanting to ( Z6 X* g* _; a3 T) ?6 ^learn about the topic, but also those experienced analytical chemists # k& z2 h3 d# T3 k9 n( vwho are still inspired by their profession./ v6 ^' [. l0 D9 p

The contents provide for easy reading by using natural products m0 {+ x" _+ q2 @: V that everyone knows, such as caffeine, backed by an attractive layout* L x, F) H; A, D- ]6 p. W' j with many pictures to visualize the topics.6 m# m/ ?) X1 o- t) B8 J

In addition, an in-depth analytical part makes the book a , T* g' C, x8 hvaluable teaching tool, or for self-learning using the questions and 9 m. k2 Z( ]: F% B0 P" lanswers at the end of each chapter.


Table of Contents:

Preface.) D+ [ D' w u 0 \: `8 i9 Q/ @3 s3 v& I

8 \ W2 m3 Z$ n9 V: sALKALOIDS. * Y, a7 u- H; }7 R: R t7 L8 c' R, }9 k3 r1 [

* Y( B0 ^; G% h B! y# qNicotine.( x# F' `6 p: j$ N % i& }( ^" {8 F8 j) J

$ x- M2 f6 D' [' ]1 gCaffeine. % a9 {9 z2 V: L% c* N3 m 4 j2 I. }& C4 V: G# P$ E

1 u/ c( |2 K r- kTheobromine. 6 b: W" }: e/ a) T+ Y) D* \, a) J; u6 U+ r h& w2 o% P E( o

* Y1 j' \. }" |# @9 R Piperine.; J, R& h |" V& T( e 0 j- L8 w# b) ]+ N( O4 W$ C% C. \2 v

( Q& A+ [% d7 D Cytisine.4 B1 o7 c3 g, |8 ^1 j' |" { : n, ?5 E: E8 w! _

5 e$ i% L) O. q# H' `% u Galanthamine. ) C, M% \% t: y# W2 r/ `( ]; X. v% ?7 V6 p

3 r2 L; g, _: a Strychnine. , ?, P/ q4 V8 ?- {" M) h7 r: i1 O % E, _+ l4 z# G3 Y

# x6 R! } Z" d; m0 s: LAROMATIC COMPOUNDS. 8 |) _' v( ?" U) C! |3 s: Z$ K" \9 M7 a- |) K3 N: G8 R

) s" s+ z7 V0 ~8 Q" O Anethole. ( ]* M; s- z% ~5 T$ u6 L9 T1 p/ e6 J) O3 t" r! Q

0 ?" g" S; q8 S6 ~1 s) f4 M: IEugenol.6 ?6 c7 ]5 l* ? . O) G$ X4 B6 Y4 ]

% L4 U: ]- j. V/ jChamazulene. 2 I, k. Q3 Y8 Z9 Z4 ] 0 i: q ~( ~" V+ |3 X& Z

) @3 P- w8 o/ ^2 H- M4 a% A& S3 ZTetrahydrocannabinol.4 `" K' Q8 r9 X8 b. [. ^/ k# R- y9 _ " j Z5 c2 ?* `7 o* f

l; U3 P$ G2 T3 GDYESTUFFS AND COLOURED COMPOUNDS.' K7 F5 a9 Z5 W4 B' z 4 K. m! Z3 j$ x; x0 B

7 i+ r4 D$ G' P2 r4 W0 ?, d- l7 TLawsone. ( \7 e# f4 R- i9 X% ` I% N& R$ {+ b+ c: H$ N

8 _3 L+ l; n1 E }% ^! P Curcumin. $ ^# q! b# e- X* O$ Z, \9 [2 Y+ B# K, Q! B' @. t" t ]: r

, I; a ?7 j. i# qBrazileine. # e" w7 {$ \0 k) n 9 e. k! v: Y9 X4 V- g0 y2 S$ s }* Y- |

+ l! p. \4 X7 e% N8 g" i" wIndigo. & U2 f- w9 s; c2 {) f7 k * |) e( K. @ N! k! L a! b4 z, T

% m- U7 Y2 e7 |" ?/ x; |1 tCapsanthin.- Y# _) K( ~) `5 @) D; c/ j ! P9 j7 v3 ?3 V5 X

+ o* k" j, K! {+ r CARBOHYDRATES. + ~$ k# c4 _1 T) D u7 {& j. s( x" {% c

0 o9 \% ]6 @3 D0 eGlucosamine.+ {$ @0 b x$ M* F, G 2 ~- \1 J4 e4 c% h7 [

6 c% z9 ]6 R9 FLactose.2 J6 Y5 _( @* Z+ z8 i 5 ~$ c/ D- z$ O% c& `8 z

) h0 n6 h0 L/ g* X. m6 nAmygdalin. 4 k Y& }. J, y+ \" f& O0 e6 `/ w0 G: @7 t, x

# p& L6 _! B" U. z& ~$ E% F! X Hesperidin.7 K$ ~3 p, |, Q C$ Z , W9 }. o6 u6 L5 x) u

: M- t, J1 o/ Z- Q8 C: g0 nTERPENOIDS., Y0 W" U5 ~) r4 {3 Q2 q% @ 1 k$ Y* w/ I1 [# E. [% R. \. Q

: |! G r4 V' o, m$ [Limonene.# J. l7 v% G% l$ s/ A ) V: U ?- M% {* F( e3 Q

8 Z. ?4 V8 e) W% H5 m) E3 x; V Menthol.3 F) d' z8 g6 W% _ 0 l# s0 y: D) M* Y/ U: j

& m( G7 L5 b; q X8 G w) b5 [ The Thujones.- u. T# D5 `. L5 E : k9 N& ~7 x/ U% a# @2 E2 M+ u

/ W9 [, G) l9 n; d& NPatchouli Alcohol.% H& }! Q3 [; x( X: j 3 R! @/ I4 V# A [

K0 C" y. k! w; |0 y Onocerin.4 c& b7 b& U2 q v# W $ _. ?- @! A! f- u& d1 a3 I- H

7 M% q0 c; D9 |% ^4 b Cnicin. 2 b$ G8 ]' A K+ N % h% ^3 f2 t* b4 ]1 W7 U

_& S' P# {# R; f Abietic Acid. [8 R9 A2 n. k 9 a2 X5 o2 T& W* a5 E

5 [! s/ ?. |. hBetulinic Acid.& Z# \+ B0 m2 [; h2 O+ f I& K. ~ 7 k. n) e" Z+ o, h% q6 p

. `( r7 Y2 V; l5 K! A; o' ?( hMISCELLANEOUS. * p$ \, G. n7 ?% X$ x% C0 Z: N ; E6 t; b+ H- j# i; F# r: b

p0 ^: e1 [6 }' ~" }Shikimic Acid. ; A( X' b4 }- u: b " F+ K' x. \& Z% k/ M

3 m! i3 _7 ^# q' w' Z) S7 V+ W Aleuritic Acid.: w$ W# [ g; F- `* f 6 P O2 \' i( J: R: T! {

) U( S' C# U1 d9 }ANSWERS TO QUESTIONS AND TRANSLATIONS. $ l7 H4 P0 g% o8 \! X+ B2 Q [8 `# P0 |% A' W! M2 s0 }+ ?/ V

( j1 `9 n u8 m$ I- z; N! N9 c7 E% bAppendix.


Author Information:

Stefan Berger
is 1 @) y: J, q# m [8 U1 Wprofessor for structural analytics at the University of Leipzig.7 d2 a% O g# b7 E Besides his many publications he wrote and edited several books among; I4 X" w; ~/ {# b& r: I them 100/150/200 and more basic NMR Experiments, NMR Spectroscopy of0 c9 |7 b y& j) N8 E( j* i non-metals, and 13C-NMR-Spectroscopy. ' O) i5 X" S: S+ N

7 d! @5 X; y6 O) \& a; _Dieter Sicker is adjunct professor at the University of Leipzig. # {7 O8 g+ n: s5 O3 K! v' s& |His current research involves him in natural product and heterocycles $ x% h6 O- v# dsynthesis and carbohydrate chemistry., d2 d1 h" b% A! l/ f* H5 z, ~


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发表于 2009-10-20 23:08:32 | 显示全部楼层
"describe the art of NMR using everyday& r, T; }' g4 I/ t examples!"--- 网上有电子版.


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[此贴子已经被作者于2009-10-20 23:12:20编辑过]
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