13C NMR data for chlorine- or nitro-substituted azomethine dyes
The 13C NMR spectra of 1‐aryl‐substituted 3‐methyl‐2‐pyrazolin‐5‐ones and their azomethine dyes have been recorded and assigned. ortho‐Substituents (Cl and NO2) on the phenyl ring in the 1‐position of the pyrazoline moiety show a small influence on the chemical shift of the azomethine bond carbon at...
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| Veröffentlicht in: | Magnetic resonance in chemistry 1990-09, Vol.28 (9), p.817-819 |
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| container_issue | 9 |
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| container_title | Magnetic resonance in chemistry |
| container_volume | 28 |
| creator | Haessner, Rainer Hennig, Lothar Gaca, Jerzy |
| description | The 13C NMR spectra of 1‐aryl‐substituted 3‐methyl‐2‐pyrazolin‐5‐ones and their azomethine dyes have been recorded and assigned. ortho‐Substituents (Cl and NO2) on the phenyl ring in the 1‐position of the pyrazoline moiety show a small influence on the chemical shift of the azomethine bond carbon atom, C‐4. |
| doi_str_mv | 10.1002/mrc.1260280915 |
| format | Article |
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Reson. Chem</addtitle><description>The 13C NMR spectra of 1‐aryl‐substituted 3‐methyl‐2‐pyrazolin‐5‐ones and their azomethine dyes have been recorded and assigned. ortho‐Substituents (Cl and NO2) on the phenyl ring in the 1‐position of the pyrazoline moiety show a small influence on the chemical shift of the azomethine bond carbon atom, C‐4.</description><subject>1-Aryl-substituted 3-methyl-2-pyrazolin-5-ones and their azomethine dyes</subject><subject>13C NMR</subject><subject>Atomic and molecular physics</subject><subject>Exact sciences and technology</subject><subject>Molecular properties and interactions with photons</subject><subject>Nuclear resonance and relaxation</subject><subject>Physics</subject><subject>Substituent effects</subject><issn>0749-1581</issn><issn>1097-458X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNpFkN1LwzAUxYMoOKevPvfFx8ybpGmSJ9GiU-imDD_2FtI2YdFuHUmHzr_eysTBhcvhnt_lcBA6JzAiAPRyGaoRoRlQCYrwAzQgoAROuZwfogGIVGHCJTlGJzG-A4BSgg3QFWF5Mp3Mktp0JnFtSKpF0wa_sjjpxcp3ocVxU8bOd5vO1on5bpe2W_SGpN7aeIqOnGmiPfvbQ_Ryd_uc3-PicfyQXxfYEyI5JnXVjyTMWVX2abPUMZZRp5gCARWUJa0trU2accVSoMAICCOoVLwkzjg2RBe7v2sTK9O4YFaVj3od_NKErSaKAeVE9j618336xm73d9C_Hem-I73vSE9m-V71LN6xPnb265814UNnggmu36ZjLW9eRfFUCD1nP389ajY</recordid><startdate>199009</startdate><enddate>199009</enddate><creator>Haessner, Rainer</creator><creator>Hennig, Lothar</creator><creator>Gaca, Jerzy</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope></search><sort><creationdate>199009</creationdate><title>13C NMR data for chlorine- or nitro-substituted azomethine dyes</title><author>Haessner, Rainer ; Hennig, Lothar ; Gaca, Jerzy</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i1185-1dc1dc813fe9b10064f3362f939070c0bb2de2da4659340203107a72895b1faf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>1-Aryl-substituted 3-methyl-2-pyrazolin-5-ones and their azomethine dyes</topic><topic>13C NMR</topic><topic>Atomic and molecular physics</topic><topic>Exact sciences and technology</topic><topic>Molecular properties and interactions with photons</topic><topic>Nuclear resonance and relaxation</topic><topic>Physics</topic><topic>Substituent effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haessner, Rainer</creatorcontrib><creatorcontrib>Hennig, Lothar</creatorcontrib><creatorcontrib>Gaca, Jerzy</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><jtitle>Magnetic resonance in chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haessner, Rainer</au><au>Hennig, Lothar</au><au>Gaca, Jerzy</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>13C NMR data for chlorine- or nitro-substituted azomethine dyes</atitle><jtitle>Magnetic resonance in chemistry</jtitle><addtitle>Magn. Reson. Chem</addtitle><date>1990-09</date><risdate>1990</risdate><volume>28</volume><issue>9</issue><spage>817</spage><epage>819</epage><pages>817-819</pages><issn>0749-1581</issn><eissn>1097-458X</eissn><coden>MRCHEG</coden><abstract>The 13C NMR spectra of 1‐aryl‐substituted 3‐methyl‐2‐pyrazolin‐5‐ones and their azomethine dyes have been recorded and assigned. ortho‐Substituents (Cl and NO2) on the phenyl ring in the 1‐position of the pyrazoline moiety show a small influence on the chemical shift of the azomethine bond carbon atom, C‐4.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/mrc.1260280915</doi><tpages>3</tpages></addata></record> |
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| ispartof | Magnetic resonance in chemistry, 1990-09, Vol.28 (9), p.817-819 |
| issn | 0749-1581 1097-458X |
| language | eng |
| recordid | cdi_pascalfrancis_primary_19302518 |
| source | Wiley Online Library All Journals |
| subjects | 1-Aryl-substituted 3-methyl-2-pyrazolin-5-ones and their azomethine dyes 13C NMR Atomic and molecular physics Exact sciences and technology Molecular properties and interactions with photons Nuclear resonance and relaxation Physics Substituent effects |
| title | 13C NMR data for chlorine- or nitro-substituted azomethine dyes |
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