1、单击此处编辑母版标题样式,单击此处编辑母版文本样式,第二级,第三级,第四级,第五级,*,*,第四章 红外,吸收,光谱分析法,一、红外谱图解析,analysis of,infrared spectrograph,二、未知物结构确定,structure determination of compounds,第四节 红外谱图解析,infrared absorption spec-,troscopy,,IR,analysis of,infrared spectrograph,2025/12/27 周六,一,、红外谱图解析,analysis of,infrared spectrograph,1烷烃,(,
2、CH,3,,CH,2,,CH)(CC,CH),-(,CH,2,),n-,n,as,1460,cm,-1,s,1380,cm,-1,CH,3,CH,2,s,1465,cm,-1,CH,2,r,720 cm,-1,(,水平摇摆),重叠,CH,2,对称伸缩2853,cm,-1,10,CH,3,对称伸缩2872,cm,-1,10,CH,2,不对称伸缩2926,cm,-1,10,CH,3,不对称伸缩2962,cm,-1,10,3000,cm,-1,2025/12/27 周六,H,C,1,3,8,5,-,1,3,8,0,c,m,-,1,1,3,7,2,-,1,3,6,8,c,m,-,1,C,H,3,C,H
3、3,CH,3,s,CC,骨架振动,1:1,1155,cm,-1,1170,cm,-1,C,C,H,3,C,H,3,1,3,9,1,-,1,3,8,1,c,m,-,1,1,3,6,8,-,1,3,6,6,c,m,-,1,4:5,1195,cm,-1,C,C,H,3,C,H,3,C,H,3,1,4,0,5,-,1,3,8,5,c,m,-,1,1,3,7,2,-,1,3,6,5,c,m,-,1,1:2,1250,cm,-1,a),由于支链的引入,使,CH,3,的对称变形振动发生变化。,b),CC,骨架振动,明显,2025/12/27 周六,c),CH,2,面外变形振动,(,CH,2,),n,,,证
4、明长碳链的存在。,n,=1,770785,cm,-1,(,中,),n,=2,740 750,cm,-1,(,中,),n,=3,730 740,cm,-1,(,中,),n,722,cm,-1,(,中强,),d),CH,2,和,CH,3,的相对含量也可以由,1460,cm,-1,和,1380,cm,-1,的峰,强度估算,强度,cm,-1,1500,1400,1300,正二十八烷,cm,-1,1500,1400,1300,正十二烷,cm,-1,1500,1400,1300,正庚烷,2025/12/27 周六,2025/12/27 周六,2.烯烃,炔烃,伸缩振动,变形振动,a)C-H,伸缩振动,(,3
5、0,00,cm,-1,),3080,cm,-1,3030,cm,-1,3080,cm,-1,3030,cm,-1,3300,cm,-1,(C-H),3080-3030,cm,-1,2900-2800,cm,-1,30,00,cm,-1,2025/12/27 周六,b)C=C,伸缩振动(,1680-1630,cm,-1,),1660,cm,-1,分界线,(C=C),反式烯,三取代烯,四取代烯,1680-1665,cm,-1,弱,尖,顺式烯,乙烯基烯,亚乙烯基烯,1660-1630,cm,-1,中强,尖,2025/12/27 周六,分界线,1660,cm,-1,顺强,反弱,四取代(不与,O,N,等
6、相连)无,(C=C),峰,端烯的强度强,共轭使,(C=C),下降20-30,cm,-1,2140-2100,cm,-1,(弱),2260-2190,cm,-1,(弱),总结,2025/12/27 周六,c)C-H,变形振动(,1000-700,cm,-1,),面内变形,(=,C-H),1400-1420,cm,-1,(,弱),面外变形,(=,C-H),1000-700,cm,-1,(,有价值),(=,C-H),970,cm,-1,(,强),790-840,cm,-1,(820,cm,-1,),610-700,cm,-1,(,强),2:,1375-1225,cm,-1,(,弱),(=,C-H),
7、800-650,cm,-1,(,690,cm-,1,),990,cm,-1,910,cm,-1,(,强),2:,1850-1780,cm,-1,890,cm,-1,(,强),2:,1800-1780,cm,-1,2025/12/27 周六,谱图,2025/12/27 周六,2025/12/27 周六,对比,烯烃顺反异构体,2025/12/27 周六,3.醇(,OH),O,H,C,O,a)-OH,伸缩振动,(3600,cm,-1,),b),碳氧伸缩振动,(1100,cm,-1,),游离醇,酚,伯-,OH,3640,cm,-1,仲-,OH,3630,cm,-1,叔-,OH,3620,cm,-1,酚
8、OH,3610,cm,-1,(,OH),(,C-O,),1050,cm,-1,1100,cm,-1,1150,cm,-1,1200,cm,-1,支化,:-15,cm,-1,不饱和,:-30,cm,-1,2025/12/27 周六,OH,基团特性,双分子缔合(二聚体),3550-3450,cm,-1,多分子缔合(多聚体),3400-3200,cm,-1,分子内氢键:,分子间氢键:,多元醇(如1,2-二醇),3600-3500,cm,-1,螯合键(和,C=O,NO,2,等),3200-3500,cm,-1,多分子缔合(多聚体),3400-3200,cm,-1,分子间氢键随浓度而变,而分子内氢键
9、不随浓度而变。,水(溶液),3710,cm,-1,水(固体),3300,cm-1,结晶水,3600-3450,cm,-1,2025/12/27 周六,3515,cm,-1,001,M,01M,025M,10M,3640,cm,-1,3350,cm,-1,乙醇在四氯化碳中不同浓度的,IR,图,2950,cm,-1,2895,cm,-1,2025/12/27 周六,2025/12/27 周六,2025/12/27 周六,脂族和环的,C-O-C,as,1150-1070,cm,-1,芳族和乙烯基的=,C-O-C,as,1275-1200,cm,-1,(,1250,cm,-1,),s,1075-102
10、0,cm,-1,4.,醚(,COC),脂族,R-OCH,3,s,(CH,3,),2830-2815,cm,-1,芳族,Ar-OCH,3,s,(CH,3,),2850,cm,-1,2025/12/27 周六,5醛、酮,2025/12/27 周六,醛,2025/12/27 周六,2025/12/27 周六,6羧酸及其衍生物,羧酸的红外光谱图,2025/12/27 周六,酰胺的红外光谱图,2025/12/27 周六,不同酰胺吸收峰数据,2025/12/27 周六,酸酐和酰氯的红外光谱图,2025/12/27 周六,氰基化合物的红外光谱图,CN,=2275-2220cm,-1,2025/12/27 周
11、六,硝基化合物的红外光谱图,AS(N=O),=1565-1545cm,-1,S(N=O),=1385-1350cm,-1,脂肪族,芳香族,S(N=O),=1365-1290cm,-1,AS(N=O),=1550-1500cm,-1,2025/12/27 周六,二、未知物结构确定,structure determination of compounds,1.未知物,2025/12/27 周六,2.推测,C,4,H,8,O,2,的结构,解:1),=1-8/2+4=1,2),峰归属,3)可能的结构,2025/12/27 周六,3.推测,C,8,H,8,纯液体,解:1),=1-8/2+8=5,2),峰
12、归属,3)可能的结构,2025/12/27 周六,4.,C,8,H,7,N,,确定结构,解:1),=1-(1-7)/2+8=6,2),峰归属,3)可能的结构,2025/12/27 周六,内容选择:,第一节 红外基本原理,basic principle of,Infrared absorption spectroscopy,第二节 红外光谱与分子结构,infrared spectroscopy,and molecular structure,第三节 红外光谱仪器,infrared absorption spectrophotometer,第四节 红外谱图解析,analysis of,Infrared spectrograph,第五节 激光拉曼光谱,laser Raman spectrometry,结束,2025/12/27 周六,






