SINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA

Radioiodine compounds have been used in nuclear medicine, industry and hydrology. Usually, radioiodine compounds are synthesized by isotopic exchange reaction. In the present works, o-iodobenzoic acid and p-iodoanisole had been synthesized by the thalation reaction of benzoicacid and anisole followe...

Full description

Saved in:
Bibliographic Details
Main Author: Syaawalz, Amry
Format: Theses
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/2009
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:2009
spelling id-itb.:20092004-11-21T04:13:54ZSINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA Syaawalz, Amry Indonesia Theses INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/2009 Radioiodine compounds have been used in nuclear medicine, industry and hydrology. Usually, radioiodine compounds are synthesized by isotopic exchange reaction. In the present works, o-iodobenzoic acid and p-iodoanisole had been synthesized by the thalation reaction of benzoicacid and anisole followed by iodination. By using this method o-iodobenzoic acid and p-iodoanisole were obtained in 23,2% and 78,0%, respectively. A reaction of resorcinolthalium bistrifluoroacetic and benzoylchloride had also been carried out. Liquid chromatographic analysis of the reaction product indicated a mixture of three different compounds. The retention time of the first compound was 1,7 minuttes, the second was 2,2 minuttes and the third one was 5,8 minuttes. The melting point of these compound were 114°C, 134°C and 116°C, respectively. The infrared and nuclear magnetic resonance spectroscopic analysis showed that all of these compounds had the characteristics of the aromatic absorbtion and difference absorbtion of the carbonyl functions. The stucture of these compounds had not yet been fur ther elucidated. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Radioiodine compounds have been used in nuclear medicine, industry and hydrology. Usually, radioiodine compounds are synthesized by isotopic exchange reaction. In the present works, o-iodobenzoic acid and p-iodoanisole had been synthesized by the thalation reaction of benzoicacid and anisole followed by iodination. By using this method o-iodobenzoic acid and p-iodoanisole were obtained in 23,2% and 78,0%, respectively. A reaction of resorcinolthalium bistrifluoroacetic and benzoylchloride had also been carried out. Liquid chromatographic analysis of the reaction product indicated a mixture of three different compounds. The retention time of the first compound was 1,7 minuttes, the second was 2,2 minuttes and the third one was 5,8 minuttes. The melting point of these compound were 114°C, 134°C and 116°C, respectively. The infrared and nuclear magnetic resonance spectroscopic analysis showed that all of these compounds had the characteristics of the aromatic absorbtion and difference absorbtion of the carbonyl functions. The stucture of these compounds had not yet been fur ther elucidated.
format Theses
author Syaawalz, Amry
spellingShingle Syaawalz, Amry
SINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA
author_facet Syaawalz, Amry
author_sort Syaawalz, Amry
title SINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA
title_short SINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA
title_full SINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA
title_fullStr SINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA
title_full_unstemmed SINTESA ARILYODIDA MELALUI ARILTALIUM DAN PENGGUNAAN ARILTALIUM UNTUK SINTESA
title_sort sintesa arilyodida melalui ariltalium dan penggunaan ariltalium untuk sintesa
url https://digilib.itb.ac.id/gdl/view/2009
_version_ 1820663128943230976