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Usage

Uses

Used in Organic Synthesis:
N-2,6-Diisopropylphenylpyridin-2-aldimin is used as a building block for the production of various other chemicals and materials. Its versatile structure allows for the creation of a wide range of compounds with different properties and applications.
Used in Coordination Chemistry:
N-2,6-Diisopropylphenylpyridin-2-aldimin is used as a ligand in coordination chemistry, where it can form complexes with metal ions. These complexes can have unique properties and can be used in various applications, such as catalysts or sensors.
Used in Catalysis Reactions:
N-2,6-Diisopropylphenylpyridin-2-aldimin can also be used as a ligand in catalysis reactions, where it can help to increase the efficiency and selectivity of certain chemical processes. This can be particularly useful in the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Overall, N-2,6-Diisopropylphenylpyridin-2-aldimin is a highly versatile compound with potential applications across different industries, including pharmaceuticals, materials science, and chemical manufacturing.

Upstream product

• 1121-60-4 pyridine-2-carbaldehyde 
• 24544-04-5 2,6-diisopropylbenzenamine 

Downstream Products

• 263254-74-6 N-(2,6-diisopropylphenyl)-N-(pyridin-2-ylmethyl)amine 

Relevant academic research and scientific papers

Silver(I)-pyridinyl Schiff base complexes: Synthesis, characterisation and antimicrobial studies

Fifteen new silver(I)-pyridinyl complexes of the general formula [AgL2]X, where X = ClO4?, OTf or NO3?, were synthesised by reacting (E)-N-(pyridinylmethylene)aniline ligands and the respective silver

Silver(I)-pyridinyl Schiff base complexes: Synthesis, structural characterization and reactivity in ring-opening polymerisation of ε-caprolactone

Reactions of AgO2C2F3with 2-pyridinyl Schiff base ligands bore five novel complexes of the type [(AgO2C2F3)2.L2]: where L?=?L1, (E)-N-(1-(pyridin-2-yl)ethylidene)anili

PYRIDINE COMPLEX OF ZIRCONIUM, CATALYTIC SYSTEM COMPRISING SAID PYRIDINE COMPLEX OF ZIRCONIUM AND PROCESS OF (CO)POLYMERIZATION OF CONJUGATED DIENES

Pyridine complex of zirconium having general formula (I): ? Said pyridine complex of zirconium having general formula (I) may advantageously be used in a catalytic system for the (co)polymerization of conjugated dienes.

(E)-N-(Pyridine-2-ylmethylene)arylamine as an Assembling Ligand for Zn(II)/Cd(II) Complexes: Aryl Substitution and Anion Effects on the Dimensionality and Luminescence Properties of the Supramolecular Metal-Organic Frameworks

Using five Schiff base ligands (E)-N-(pyridine-2-yl) (CH=NPhR) (where R = 4-CH3, L1; 2,6-(CH3)2, L2; 2,4,6-(CH3)3, L3; 2,6-(C2H5)2, L4; 2,6-(i-C3H7)2, L5), nine Zn(II)/Cd(II) complexes, namely, Zn1-Zn3, Cd1, Cd2, Cd3a, Cd3b, Cd4, and Cd5, have been successfully synthesized. The structures of the Zn(II)/Cd(II) complexes have been established by single crystal X-ray diffraction and further physically characterized by 1H NMR, FT-IR, and elemental analysis. The crystal structures of these complexes indicate that the structures of ligand and anions can directly influence the formation of 1D → 3D supramolecular metal-organic frameworks (SMOFs) via C-H···O/C-H···Cl hydrogen bonds and π···π interactions. Upon irradiation with UV light, the nine Zn(II)/Cd(II) complexes display deep blue emissions of 401-436 nm in acetonitrile solution and light blue or bluish green emissions of 485-575 nm in the solid state, respectively. The photoluminescence properties of nine Zn(II)/Cd(II) complexes can be finely and predictably tuned over a wide range of wavelengths by small and easily implemented changes to ligand structure. It is worth noting that Zn1 and Cd1 exhibit obvious aggregation-induced emission enhancement (AIEE) properties in the CH3CN-H2O mixture solutions.

Topological Evolution in Mercury(II) Schiff Base Complexes Tuned through Alkyl Substitution – Synthesis, Solid-State Structures, and Aggregation-Induced Emission Properties

From two series of Schiff base ligands, (E)-N-(pyridine-2-yl)(CMe=NPhR) and (E)-N-(pyridine-2-yl)(CH=NPhR) [R = H, L1a, L1b; 2-CH3, L2a, L2b; 4-CH3, L3a, L3b; 2,6-(CH3)2, L4a, L4b; 2,6-(C2H5/sub

A strategy for the synthesis of well-defined iron catalysts and application to regioselective diene hydrosilylation

We report the development of a well-defined Fe catalyst and its application to the regio-and stereoselective 1,4-hydrosilylation of 1,3-dienes. To the best of our knowledge, this is the first example of accessing a characterized low-valent Fe catalyst by controlled reductive elimination from a readily accessible Fe precatalyst.

Iron-catalyzed 1,4-hydroboration of 1,3-dienes

(Chemical Equation Presented) A chemo-, regio-, and stereoselective iron-catalyzed 1,4-hydroboration of dienes that affords γ-disubstituted allylboranes has been developed. 1,4-Hydroboration of 2-substituted dienes forms allylborane products with (E)-trisubstituted double bonds exclusively.

Efficient activation of 2-iminomethylpyridine/cobalt-based alkyne [2+2+2] cycloaddition catalyst by addition of a silver salt

The addition of silver triflate (AgOTf) or silver hexafluoroantimonate (AgSbF6) significantly increased the activity of the 2-(arylimino)methylpyridine/cobalt(II) chloride hexahydrate (CoCl 2·6O H2O)/zinc catalyst in alkyne cyclotrimerizations thereby accelerating the reaction and enabling the use of unactivated, simple internal alkynes as the monoyne substrate : The rate of reaction was found to be highly dependent on the nature of the counter anion (X-) and the ligand (L) in the postulated cationic cobalt(I) complex [LCo(I)]+X-.

A highly practical instant catalyst for cyclotrimerization of alkynes to substituted benzenes

A 2-(2,6-diisopropylphenyl)iminomethylpyridine (1a)/CoCl 2·6H2O/Zn reagent has been developed as an effective instant catalyst for the intra- and intermolecular cyclotrimerization of alkynes to substituted benzenes, making the method

Synthesis and X-ray structures of new mononuclear and dinuclear diimine complexes of late transition metals

Synthesis of new palladium(II) (1), nickel(II) (2a and 2b), and cobalt(II) (3) complexes bearing the unsymmetrical, bidentate nitrogen ligand 2,6-bis(1-methylethyl)-N-(2-pyridinylmethylene)phenylamine (L) is described. The solidstate structures of 1, 2a,