𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and Spectroscopic Characterization of Potassium Polyfluoroalken-1-yltrifluoroborates

✍ Scribed by H.-J. Frohn; V. V. Bardin


Publisher
John Wiley and Sons
Year
2001
Tongue
German
Weight
119 KB
Volume
627
Category
Article
ISSN
0372-7874

No coin nor oath required. For personal study only.

✦ Synopsis


The potassium fluoroborates K[RCF=CFBF 3 ] (R = F, Cl (cis-/trans-mixture), trans-C 4 F 9 , cis-C 2 F 5 , cis-C 6 F 13 , trans-C 4 H 9 , trans-C 6 H 5 ) were prepared by fluoridation (methoxide-fluoride substitution with K[HF 2 ]) of RCF=CFB(OMe) 2 and Li[RCF=CFB(OMe) 3 ] which were obtained from RCF=CFLi and B(OMe) 3 . The K[RCF=CFBF 3 ] salts were characterized by their 1 H, 11 B, 19 F NMR and IR spectra.


📜 SIMILAR VOLUMES


Synthesis and Spectroscopic Characteriza
✍ Rutger B. Boers; Yolanda Pazos Randulfe; Hendrikus N. S. van der Haas; Marleen v 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB

This paper presents the synthesis of 1-13 C-and 4-13 C-plastoquinone-9 and their characterization with NMR spectroscopy and mass spectrometry. The synthetic scheme has been further adapted to introduce 13 C-labeled plastoquinones on all individual and on each combination of positions in the qui-

Synthesis and Spectroscopic Characteriza
✍ D. Chaudhuri; A. Kumar; I. Rudra; D. D. Sarma 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 181 KB

## Experimental Synthesis of Gels: The gels used in this work were synthesized from acrylic acid and acryloyl derivatives of amino acids that contain a hydrophobic alkyl chain (of length = n) and a terminal hydrophilic carboxyl group [13]. Specifically we have used acrylic acid (AAC, n = 0), acryl

Synthesis, spectroscopic characterizatio
✍ Colin L. Honeybourne; Kevin J. Barrell 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 148 KB 👁 1 views

The synthesis of three novel porphyrins (that are models for mesoporphyrin) requires the synthesis of eight new pyrroles, one new alkyl-3-oxohexanoate and two new dipyrromethanes. The new porphyrin free bases have hydrophobic substitution patterns different from that in mesoporphyrin. We are seeking