𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H and 13C NMR study of paramagnetic chiral macrocyclic lanthanide complexes

✍ Scribed by Jerzy Lisowski


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
129 KB
Volume
37
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


The chiral macrocyclic complexes obtained in a template condensation of (R,R)-1,2-diaminocyclohexane and 2,6-diformylpyridine, Ln \ La(III), Ce(III), Eu(III) and Yb(III), were studied by 1H [LnL](NO 3 ) 3 , and 13C NMR spectroscopy. The signal assignment was based on COSY, NOESY and HMQC measurements and the isotropic shifts of the paramagnetic complexes were analysed. The spectra of the investigated compounds in methanolÈchloroform solution indicate a helical conformation of the ligand. The chiral D 2 -symmetrical, complexes are able to form diastereoisomeric adducts with D-and L-aminoacids that can be distin-[LnL](NO 3 ) 3 guished by 1H NMR spectroscopy.


📜 SIMILAR VOLUMES


Spectral Discrimination of Chiral Macroc
✍ Silvio Aime; Mauro Botta; Simonetta Geninatti Crich; Enzo Terreno; Pier Lucio An 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 127 KB

The anionic lanthanide(iii) complexes of the macrocyclic ligand 1,4,7,10-tetraazacyclododecane-N,N',N'',-N'''-tetramethylenephosphonate (DOTP) are present in aqueous solution as a racemic mixture of two enantiomeric forms interconverting slowly on the NMR time scale. The metal chelates form diastero

1H and 13C NMR study of copteroside E de
✍ Carlos M. Cerda-García-Rojas; Graciela Zamorano; María Isabel Chávez; César A. N 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 181 KB 👁 2 views
1H and 13C NMR Studies of Some Anthraqui
✍ K. Danielsen; G. W. Francis; D. W. Aksnes 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 297 KB 👁 2 views

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

1H and 13C NMR study of quaternary benzo
✍ Radek Marek; Jaromír Toušek; Jiří Dostál; Jiří Slavík; Roger Dommisse; Vladimír 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 105 KB 👁 2 views

C and in some cases also 15 N chemical shifts of quaternary benzo[c]phenanthridine alkaloids (fagaronine, chelerythrine, chelilutine, chelirubine, nitidine, sanguilutine, sanguinarine, and sanguirubine) were systematically studied by NMR spectroscopy and ab initio calculations. The assignment of sig

13C- and 1H-nmr studies of cis-trans con
✍ Yen-Yau H. Chao; R. Bersohn 📂 Article 📅 1978 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 321 KB 👁 2 views

In aqueous solutions, 13C-and 'H-nmr studies show that the percentage of trans conformation of proline oligomers +H\*N Pro-(Pro),-CO; increases substantially from n = 1 (65% trans) t o n = 2 (90% trans). The relatively low percentage of trans structure for the dimer ( n = 1) very likely is caused by