✦ LIBER ✦

Separation of aliphatic and aromatic amines by the ion interaction reagent RP-HPLC technique

✍ Scribed by M. C. Gennaro; E. Marengo

Book ID: 112733048
Publisher: Springer
Year: 1988
Tongue: English
Weight: 361 KB
Volume: 25
Category: Article
ISSN: 0009-5893
DOI: 10.1007/bf02327655

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The use of chiral interaction reagents i

The use of chiral interaction reagents in the separation of D(−)-and L(+)-ascorbic acid by ion interaction reversed-phase HPLC

✍ M. C. Gennaro; C. Abrigo; E. Marengo 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 491 KB

Role of the alkyl chain length of the io

Role of the alkyl chain length of the ion interaction reagent, flow-rate, column packing and detection in ion interaction reversed-phase high-performance liquid chromatography in separations of anions using amine salicylates

✍ M.C. Gennaro 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 598 KB

The separation of aliphatic amines in di

The separation of aliphatic amines in dilute aqueous solution by gas chromatography and application of this technique to the quantitative analysis of tri- and dimethylamine in fish

✍ J. N. Keay; R. Hardy 📂 Article 📅 1972 🏛 John Wiley and Sons 🌐 English ⚖ 602 KB

Study of the interaction of hexa-amine c

Study of the interaction of hexa-amine cobalt (III) ion with DNA by a resonance light scattering technique and its analytical application

✍ Zheng-ping Li; Yan-kun Li; Yu-cong Wang 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB 👁 2 views

Radical anion and Meisenheimer complexes

Radical anion and Meisenheimer complexes arising from interaction of the hydroxyl ion or aliphatic amines with photoexcited 4-nitroveratrole studied by electron spin resonance and time-resolved resonance Raman scattering

✍ Alexander M.J. van Eijk; A. Herbert Huizer; Cyril A.G.O. Varma 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 816 KB

An electron spin resonance study of the reaction of aliphatic amines and OH-with 4nitroveratrole (NV) in its lowest electronic triplet state is presented. It is concluded that both nucleophiles transfer an electron to triplet-state NV in the first chemical step of the reaction. This is then followed