1403/02/08
محمد قادرمزی

محمد قادرمزی

مرتبه علمی: استاد
ارکید:
تحصیلات: دکترای تخصصی
اسکاپوس: 17345456400
دانشکده: دانشکده علوم پایه
نشانی:
تلفن: 0871-6624133

مشخصات پژوهش

عنوان
Tris(piperazinediium)bis[tris(pyridine-2,6-dicarboxylato)neodymate(III)] 15.33-hydrate
نوع پژوهش
JournalPaper
کلیدواژه‌ها
Piperazinediium
سال
2008
مجله ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE
شناسه DOI
پژوهشگران zohreh Derikvand ، Hossein Aghabozorg ، Andya NEmati ، Mohammad Ghadermazi ، Jafar Attar Gharamaleki

چکیده

The title compound, (C4H12N2)3[Nd(C7H3NO4)3]215.33H2O or (pipzH2)3[Nd(pydc)3]215.33H2O (in which pipz is piperazine and pydcH2 is pyridine-2,6-dicarboxylic acid), was synthesized by the reaction of NdCl36H2O with the protontransfer compound (pipzH2)(pydc) in aqueous solution. The nine donor atoms of the three pydc2 ligands form a distorted tricapped trigonal–prismatic arrangement around the NdIII center. Considerable C—O   stacking interactions between CO groups of carboxylate fragments and aromatic rings of pydc2 with distances of 3.135 (5)–3.255 (5) A ° are observed. In the crystal structure, a wide range of hydrogen-bonding [of the types O—H  O, N—H  O and C—H  O, with D  A distances ranging from 2.608 (10) to 3.278 (7) A ° ], ion-pairing and C—O   stacking interactions connect the various components into a supramolecular structure. There is a high degree of solvent disorder in the structure; the occupancies of five water molecules refined to 0.6, 0.5, 0.4, 0.25 and 0.25