Mesoporous KIT-۶ as a support for the immobilization of a palladiumorganometallic nanocatalyst and its application in C–C coupling reactions

Publish Year: 1402
نوع سند: مقاله کنفرانسی
زبان: English
View: 92

متن کامل این Paper منتشر نشده است و فقط به صورت چکیده یا چکیده مبسوط در پایگاه موجود می باشد.
توضیح: معمولا کلیه مقالاتی که کمتر از ۵ صفحه باشند در پایگاه سیویلیکا اصل Paper (فول تکست) محسوب نمی شوند و فقط کاربران عضو بدون کسر اعتبار می توانند فایل آنها را دریافت نمایند.

  • Certificate
  • من نویسنده این مقاله هستم

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

IICC22_113

تاریخ نمایه سازی: 5 آذر 1402

Abstract:

Many Pd complexes have been used as homogeneous catalysts in cross-coupling reactions [۱].Although some of the Pd complexes have potential for recycling [۲,۳], most of them have problemssuch as deactivation and difficult separation from the solution. Thus, it is necessary to developheterogeneous catalysts which can easily be recovered from the reaction system and reused [۴, ۵].Recently, Ryoo and co-workers reported a new cubic mesoporous silica material named KIT-۶,which was prepared using triblock copolymer (P۱۲۳) as the mesopore directing agent. KIT-۶possesses large readily tunable pores with thick pore walls, high thermal stability, high specificsurface area and large pore volume. Therefore, mesoporous KIT-۶ can be used as a support for thesynthesis heterogeneous catalysts. In this work, a new Schiff base complex of Pd(II) was fabricatedon the surface of KIT-۶. For this purpose Schiff-base ligand was synthesized from condensationof diethylenetriamine (DETA) and salicylic aldehyde (SA). In the next step, Schiff-base ligandwas reacted with (۳-iodopropyl)trimethoxy silane (IPTMS). Then, Schiff base complex ofpalladium was synthesized using a complexation reaction of Pd(OAc)۲. Finally, the obtainedpalladium complex was fixed on KIT-۶ (Pd@SA-Schiff base@KIT-۶) as a new reusable andpractical catalyst in Suzuki reaction. This catalyst was characterized using IR, BET, EDS, SEM,and TGA methods.

Authors

Manzar Akbari

Department of Chemistry, Faculty of Science, Ilam University, P. O. Box ۶۹۳۱۵۵۱۶, Ilam, Iran

Mohsen Nikoorazm

Department of Chemistry, Faculty of Science, Ilam University, P. O. Box ۶۹۳۱۵۵۱۶, Ilam, Iran

Bahman Tahmasbi

Department of Chemistry, Faculty of Science, Ilam University, P. O. Box ۶۹۳۱۵۵۱۶, Ilam, Iran

Arash Ghorbani-Choghamarani

Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamedan, Iran