## Abstract Proton‐coupled as well as noise‐decoupled ^13^C NMR spectra of several substituted naphthalenes have been studied. Complete assignments of the ^13^C signals based on selectively deuterated derivatives and on the ^13^C^1^H coupling pattern have been made. For the methoxynaphthalenes, ac
13C NMR study of Π-complex formation I. Characteristic shifts of the carbon resonances of alkenes induced by silver (I)
✍ Scribed by C.D.M. Beverwijk; J.P.C.M. van Dongen
- Book ID
- 104245379
- Publisher
- Elsevier Science
- Year
- 1972
- Tongue
- French
- Weight
- 199 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Several authors have utilized 13 C NMR spectroscopy (CMR) for the investigation of 1 organo-transition metal x-complexes . In the field of organosilver complex chemistry t some 2 CMR measurements have been reported recently by Parker and Roberts . Comparing the CMR spectra 'The saturated carbon atoms are generally shifted downfield upon coordination in the range O-5 Hz in methanol and O-20 Hz in chloroform. d Complex formation of ethylene with silver nitrate and tetrafluoroborate in methanol and with silver tetrafluoroborate in chloroform (saturated solutions) resulted in an upfield shift.
📜 SIMILAR VOLUMES
Binuclear lanthanide(III)-silver(I) f3-diketonate chelates are effective N M R shift and relaxation reagents for substrates containing one or two multiply bonded nitrogen atoms, despite the fact that some of the substrates are able to react with lanthanide chelates alone. The silver cation is bonded