Preparation and Properties of Tetrathia[n](1,1′)ferrocenophanes with Pd(BF4)2. The Metal–Metal Interaction Controlled by the Size of the Thiamacrocycles

1,4,7,10-Tetrathia[10]-, 1,4,8,11-tetrathia[11]-, 1,5,8,12-tetrathia[12]-, and 1,5,9,13-tetrathia[13](1,1′)ferrocenophanes reacted with (CH3CN)4Pd(BF4)2 to give the corresponding 1/1 complexes in good yield. The 1H NMR spectra of the Pd(II) complexes were not rigid at room temperature, except for th...

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Published inBulletin of the Chemical Society of Japan Vol. 62; no. 11; pp. 3492 - 3497
Main Authors Sato, Masaru, Akabori, Sadatoshi
Format Journal Article
LanguageEnglish
Published Tokyo The Chemical Society of Japan 01.11.1989
Chemical Society of Japan
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Abstract 1,4,7,10-Tetrathia[10]-, 1,4,8,11-tetrathia[11]-, 1,5,8,12-tetrathia[12]-, and 1,5,9,13-tetrathia[13](1,1′)ferrocenophanes reacted with (CH3CN)4Pd(BF4)2 to give the corresponding 1/1 complexes in good yield. The 1H NMR spectra of the Pd(II) complexes were not rigid at room temperature, except for the complex of 1,4,7,10-tetrathia[10](1,1′)ferrocenophane. The 1H and 13C NMR spectra at low temperature showed that the Pd(II) complex of 1,5,9,13-tetrathia[13]ferrocenophane was a single compound, while the other three complexes were a mixture of two isomers. In the electronic spectra of the above series, the low-energy band shifted to the long-wavelength region and increased its absorbance according to the decrease in the size of the thiamacrocycle.
AbstractList Abstract 1,4,7,10-Tetrathia[10]-, 1,4,8,11-tetrathia[11]-, 1,5,8,12-tetrathia[12]-, and 1,5,9,13-tetrathia[13](1,1′)ferrocenophanes reacted with (CH3CN)4Pd(BF4)2 to give the corresponding 1/1 complexes in good yield. The 1H NMR spectra of the Pd(II) complexes were not rigid at room temperature, except for the complex of 1,4,7,10-tetrathia[10](1,1′)ferrocenophane. The 1H and 13C NMR spectra at low temperature showed that the Pd(II) complex of 1,5,9,13-tetrathia[13]ferrocenophane was a single compound, while the other three complexes were a mixture of two isomers. In the electronic spectra of the above series, the low-energy band shifted to the long-wavelength region and increased its absorbance according to the decrease in the size of the thiamacrocycle.
1,4,7,10-Tetrathia[10]-, 1,4,8,11-tetrathia[11]-, 1,5,8,12-tetrathia[12]-, and 1,5,9,13-tetrathia[13](1,1')ferrocenophanes reacted with (CH3CN)4Pd(BF4)2 to give the corresponding 1/1 complexes in good yield. The 1H NMR spectra of the Pd(II) complexes were not rigid at room temperature, except for the complex of 1,4,7,10-tetrathia[10](1,1')ferrocenophane. The 1H and 13C NMR spectra at low temperature showed that the Pd(II) complex of 1,5,9,13-tetrathia[13]ferrocenophane was a single compound, while the other three complexes were a mixture of two isomers. In the electronic spectra of the above series, the low-energy band shifted to the long-wavelength region and increased its absorbance according to the decrease in the size of the thiamacrocycle.
Author Sato, Masaru
Akabori, Sadatoshi
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Keywords Cyclophane
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Snippet 1,4,7,10-Tetrathia[10]-, 1,4,8,11-tetrathia[11]-, 1,5,8,12-tetrathia[12]-, and 1,5,9,13-tetrathia[13](1,1′)ferrocenophanes reacted with (CH3CN)4Pd(BF4)2 to...
Abstract 1,4,7,10-Tetrathia[10]-, 1,4,8,11-tetrathia[11]-, 1,5,8,12-tetrathia[12]-, and 1,5,9,13-tetrathia[13](1,1′)ferrocenophanes reacted with...
1,4,7,10-Tetrathia[10]-, 1,4,8,11-tetrathia[11]-, 1,5,8,12-tetrathia[12]-, and 1,5,9,13-tetrathia[13](1,1')ferrocenophanes reacted with (CH3CN)4Pd(BF4)2 to...
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SubjectTerms Chemistry
Coordination compounds
Exact sciences and technology
Inorganic chemistry and origins of life
Preparations and properties
Title Preparation and Properties of Tetrathia[n](1,1′)ferrocenophanes with Pd(BF4)2. The Metal–Metal Interaction Controlled by the Size of the Thiamacrocycles
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