Chemistry Department, Faculty of Sciences and Mathematics, Diponegoro University, Indonesia
BibTex Citation Data :
@article{JKSA3830, author = {Bambang Cahyono and Ismiyarto Ismiyarto and Agus Suradi and Meiny Suzery}, title = {Demetilasi Senyawa N-metilpiridinium iodida dengan Pemanasan pada Pelarut Polar Aprotik}, journal = {Jurnal Kimia Sains dan Aplikasi}, volume = {3}, number = {1}, year = {2000}, keywords = {Demetilasi; Garam Amonium Kuartener; Amina Tersier}, abstract = { Reaksi Demetilasi dengan anion iodida telah dilakukan terhadap senyawa N-Metilpiridinium Iodida. Reaksi berlangsu pada Suhu titik didih asetonitril, 82 Celsius. Analisis Produk Reaksi dengan Spktrofotometer UV-Vis, mengindikasikan bahwa reaksi demetilasi garam N-metilpiridinium iodida telah berlangsung. hasil Penelitian menunjukan bahwa amonium heterosiklik aromatik lebih mudah terdemetilasi daripada amonium heterosiklik nanoaromatik. }, issn = {2597-9914}, pages = {147--151} doi = {10.14710/jksa.3.1.147-181}, url = {https://ejournal.undip.ac.id/index.php/ksa/article/view/3830} }
Refworks Citation Data :
Reaksi Demetilasi dengan anion iodida telah dilakukan terhadap senyawa N-Metilpiridinium Iodida. Reaksi berlangsu pada Suhu titik didih asetonitril, 82 Celsius. Analisis Produk Reaksi dengan Spktrofotometer UV-Vis, mengindikasikan bahwa reaksi demetilasi garam N-metilpiridinium iodida telah berlangsung. hasil Penelitian menunjukan bahwa amonium heterosiklik aromatik lebih mudah terdemetilasi daripada amonium heterosiklik nanoaromatik.
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