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Usage

Uses

Used in Coordination Chemistry and Organometallic Complexes:
3,5-bis(1-imidazoly)pyridine is used as a bidentate ligand for [forming stable complexes with metal ions] because of its ability to chelate and stabilize metal ions, which is crucial in the synthesis and study of organometallic compounds.
Used in Catalysis:
3,5-bis(1-imidazoly)pyridine is used as a ligand in catalysis for [promoting desired reactivity in the formation of various organic and inorganic compounds] due to its capacity to influence the selectivity and efficiency of catalytic processes.
Used in Medicinal and Pharmaceutical Applications:
3,5-bis(1-imidazoly)pyridine is used as a potential component in the development of new drugs and therapeutic agents for [its potential medicinal properties], with ongoing research exploring its applications in creating novel pharmaceuticals.
Used in Research and Development:
3,5-bis(1-imidazoly)pyridine is used as a research compound for [exploring its unique properties and potential applications] in various scientific fields, including material science, supramolecular chemistry, and bioinorganic chemistry.

Upstream product

• 288-32-4 1H-imidazole 
• 625-92-3 3,5-dibromopyridine 

Downstream Products

• 1448467-24-0 [Cd(isophthalic acid)(3,5-bis(imidazole-1-yl)pyridine)(H₂O)]n 

Relevant academic research and scientific papers

Suzuki-Miyaura C-C coupling reactions catalysed by a homogeneous and nanosilica supported palladium(ii) N-heterocyclic carbene complex derived from 3,5-di(1-imidazolyl)pyridine

A new palladium N-heterocyclic carbene complex using 3,5-di(1H-imidazol-1-yl)pyridine (1) as a precursor was prepared. The complex was immobilized on 3-chloropropylated nanosilica as a support and characterized by FT-IR spectroscopy, thermogravimetric analysis, field emission scanning electron microscopy, energy dispersive X-ray analysis, transmission electron microscopy and elemental analysis. The prepared catalyst was used as a heterogeneous catalyst in the Suzuki-Miyaura coupling reactions of various aryl halides with phenylboronic acid and the corresponding biphenyls were being produced in a high yield. The catalyst was recyclable under aerobic conditions without significant loss of activity. Also, the catalytic activity of homogeneous catalyst was investigated.

Coordination polymers constructed by diverse metal centers and the rigid ligand 3,5-di(1H-imidazol-1-yl)pyridine: Synthesis, structure and properties

Six new coordination polymers, [Cu(L)2(H2O) 2](NO3)2 (1), [Cu(L)2](ClO 4)2 (2), [Cd(L)2(H2O) 2](ClO4)2 (3), [Cd(L)(OAc)2(H 2O)] (4), [Cu3(L)4(H2O) 2(SO4)](SO4)2·30H 2O (5), and [Ni(L)(H2O)3(SO4)] (6) [L = 3,5-di(1H-imidazol-1-yl)pyridine, OAc- = CH3COO -], have been prepared and characterized by X-ray diffraction, IR, elemental and thermogravimetric analyses. Complexes 1, 4 and 6 have different one-dimensional (1D) chain structures, while 2 and 4 are two-dimensional (2D) networks. The chains and layers are further linked together by hydrogen bonds to generate three-dimensional (3D) frameworks. Complex 5 is a (3,4,4)-connected 3D framework with a Point (Schlaefli) symbol of (4.82) 4(4.83.102)2(42.8 2.102). The influences of the coordination modes of the ligand L, metal center as well as the counteranion on the structures of the complexes are discussed. Furthermore, the reversible anion exchange property of 3 and the photoluminescence properties of 3 and 4 have been investigated.