## Abstract ^13^C NMR spectra for a number of furanoflavones are presented and analysed. The effects of various substituents are discussed.
A 13C-NMR and IR study of isocyanides and some of their complexes
✍ Scribed by R. W. Stephany; M. J. A. de Bie; W. Drenth
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 230 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^13^C chemical shifts and ^1^J(^14^N^13^C) coupling constants as well as stretching frequencies of the isocyano group are reported for some representative aliphatic, unsaturated and aromatic isocyanides and for two copper(I) isocyanide complexes. The results are discussed in terms of the inductive and mesomeric substituent effects on the polarisation and charge density of the CNC bonds. The marked solvent effect on the chemical shifts of the isocyano carbon hampers comparison of our data with previously reported data. The hydrogen bonding shift of this carbon in water or methanol is much smaller than previous data suggest.
📜 SIMILAR VOLUMES
## Abstract The ^13^C chemical shifts and one‐bond carbon‐hydrogen coupling constants have been obtained for some hydroxycoumarins and their corresponding acetoxy and methoxy derivatives. The changes in the one‐bond carbon‐hydrogen coupling constants resulting from the conversion of a hydroxy group
## Abstract The ^13^C NMR spectra of eight triterpenes are recorded and all carbon shifts have been assigned. The data are in agreement with the structures assigned to the rare lupanediol, lup‐20(29)‐ene‐3α,23‐diol, and other lupane triterpenes isolated from the Sri Lankan __Glochidion__ species (E
## Abstract The aromatic ^1^H‐ and ^13^C‐NMR. spectra of some metal complexes of o, o′‐dihydroxyazobenzenes are shown to be useful in distinguishing the two possible isomers (acolar and discolar) stemming from the non equivalence of the two ligating azo nitrogen atoms. The ortho aromatic carbon ato
## Abstract A new type of crown ethers containing a diphenyl ether unit has been prepared, the ring size ranging from 12 to 36. ^1^H and ^13^C NMR spectra of both free ligands and their metal‐ion complexes have been recorded. For 18‐ and 21‐membered compounds a general downfield shift was observed
H and lSC NMR chemical shifts are reported and assigned for 1,4,9,10-and 2,3,9,1 O-anthracenetetrone. In addition, NMR data are given for 2,3-dihydroxy-9, 1 O-anthraquinone, 2.3-dimethoxy-9.10anthraquinone and 1 -hydroxy-2-acetoxy-9,l O-anthraquinone, encountered during the preparation of the anthra