NMR investigations on Stannabicycloundecanes of the type RSn(CH2CH2CH2)3N

The 1H, 13C, and 119Sn NMR data of seven stannabicycloundecanes of the type RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) are reported. From 1H NMR coalescence data at low temperature the free activation enthalpies for the racemisation of...

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Veröffentlicht in:Zeitschrift für anorganische und allgemeine Chemie (1950) 1988, Vol.567 (1), p.122-130
Hauptverfasser: Mügge, C., Pepermans, H., Gielen, M., Willem, R., Tzschach, A., Jurkschat, K.
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container_issue 1
container_start_page 122
container_title Zeitschrift für anorganische und allgemeine Chemie (1950)
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creator Mügge, C.
Pepermans, H.
Gielen, M.
Willem, R.
Tzschach, A.
Jurkschat, K.
description The 1H, 13C, and 119Sn NMR data of seven stannabicycloundecanes of the type RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) are reported. From 1H NMR coalescence data at low temperature the free activation enthalpies for the racemisation of the bicyclo[3.3.3]skeleton were estimated to be 37 ± 1 kJ/mol. They are independent of the substituent R. However, it decreases when the tin atom is replaced by silicon for R = Me. NMR‐Untersuchungen an Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N Es werden 1H‐, 13C‐ und 119Sn‐NMR‐Daten von sieben Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) mitgeteilt. Aus den Protonen‐NMR‐Koaleszenzdaten bei tiefer Temperatur wird ΔG Tc* für die Racemisierung des Bicyclo[3.3.3]‐Gerüstes zu 37 ± 1 kJ/mol bestimmt. Die Werte sind unabhängig vom Substituenten R. In den entsprechenden Siliciumderivaten (R = Me) werden geringere Aktivierungsparameter gefunden.
doi_str_mv 10.1002/zaac.19885670114
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From 1H NMR coalescence data at low temperature the free activation enthalpies for the racemisation of the bicyclo[3.3.3]skeleton were estimated to be 37 ± 1 kJ/mol. They are independent of the substituent R. However, it decreases when the tin atom is replaced by silicon for R = Me. NMR‐Untersuchungen an Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N Es werden 1H‐, 13C‐ und 119Sn‐NMR‐Daten von sieben Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) mitgeteilt. Aus den Protonen‐NMR‐Koaleszenzdaten bei tiefer Temperatur wird ΔG Tc* für die Racemisierung des Bicyclo[3.3.3]‐Gerüstes zu 37 ± 1 kJ/mol bestimmt. Die Werte sind unabhängig vom Substituenten R. In den entsprechenden Siliciumderivaten (R = Me) werden geringere Aktivierungsparameter gefunden.</description><identifier>ISSN: 0044-2313</identifier><identifier>EISSN: 1521-3749</identifier><identifier>DOI: 10.1002/zaac.19885670114</identifier><identifier>CODEN: ZAACAB</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Atomic and molecular physics ; Exact sciences and technology ; Molecular properties and interactions with photons ; Nuclear resonance and relaxation ; Physics</subject><ispartof>Zeitschrift für anorganische und allgemeine Chemie (1950), 1988, Vol.567 (1), p.122-130</ispartof><rights>Copyright © 1988 Verlag GmbH &amp; Co. 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Chem</addtitle><description>The 1H, 13C, and 119Sn NMR data of seven stannabicycloundecanes of the type RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) are reported. From 1H NMR coalescence data at low temperature the free activation enthalpies for the racemisation of the bicyclo[3.3.3]skeleton were estimated to be 37 ± 1 kJ/mol. They are independent of the substituent R. However, it decreases when the tin atom is replaced by silicon for R = Me. NMR‐Untersuchungen an Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N Es werden 1H‐, 13C‐ und 119Sn‐NMR‐Daten von sieben Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) mitgeteilt. Aus den Protonen‐NMR‐Koaleszenzdaten bei tiefer Temperatur wird ΔG Tc* für die Racemisierung des Bicyclo[3.3.3]‐Gerüstes zu 37 ± 1 kJ/mol bestimmt. Die Werte sind unabhängig vom Substituenten R. 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Chem</addtitle><date>1988</date><risdate>1988</risdate><volume>567</volume><issue>1</issue><spage>122</spage><epage>130</epage><pages>122-130</pages><issn>0044-2313</issn><eissn>1521-3749</eissn><coden>ZAACAB</coden><abstract>The 1H, 13C, and 119Sn NMR data of seven stannabicycloundecanes of the type RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) are reported. From 1H NMR coalescence data at low temperature the free activation enthalpies for the racemisation of the bicyclo[3.3.3]skeleton were estimated to be 37 ± 1 kJ/mol. They are independent of the substituent R. However, it decreases when the tin atom is replaced by silicon for R = Me. NMR‐Untersuchungen an Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N Es werden 1H‐, 13C‐ und 119Sn‐NMR‐Daten von sieben Stannabicycloundecanen des Typs RSn(CH2CH2CH2)3N (1, R = Cl; 2, R = Br; 3, R = I; 4, R = OH; 5, R = SPh; 6, R = Me; 7, R = Sn(CH2CH2CH2)3N) mitgeteilt. Aus den Protonen‐NMR‐Koaleszenzdaten bei tiefer Temperatur wird ΔG Tc* für die Racemisierung des Bicyclo[3.3.3]‐Gerüstes zu 37 ± 1 kJ/mol bestimmt. Die Werte sind unabhängig vom Substituenten R. In den entsprechenden Siliciumderivaten (R = Me) werden geringere Aktivierungsparameter gefunden.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/zaac.19885670114</doi><tpages>9</tpages></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Atomic and molecular physics
Exact sciences and technology
Molecular properties and interactions with photons
Nuclear resonance and relaxation
Physics
title NMR investigations on Stannabicycloundecanes of the type RSn(CH2CH2CH2)3N
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