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- Schiff_base abstract "A Schiff base, named after Hugo Schiff, is a compound with the general structure R2C=NR' (R' ≠ H). They can be considered a sub-class of imines, being either secondary ketimines or secondary aldimines depending on their structure. The term is often synonymous with azomethine which refers specifically to secondary aldimines (i.e. RN=CR2 where R ≠ H).A number of special naming systems exist for these compounds. For instance a Schiff base derived from an aniline, where R3 is a phenyl or a substituted phenyl, can be called an anil, while bis-compounds are often referred to as salen-type compounds. The term Schiff base is normally applied to these compounds when they are being used as ligands to form coordination complexes with metal ions. Such complexes do occur naturally, for instance in Corrin, but the majority of Schiff bases are artificial and are used to form many important catalysts, such as Jacobsen's catalyst.".
- Schiff_base thumbnail Imino_Group_V.1.png?width=300.
- Schiff_base wikiPageID "522192".
- Schiff_base wikiPageLength "7608".
- Schiff_base wikiPageOutDegree "48".
- Schiff_base wikiPageRevisionID "682616094".
- Schiff_base wikiPageWikiLink Aldimine.
- Schiff_base wikiPageWikiLink Aliphatic_amine.
- Schiff_base wikiPageWikiLink Amine.
- Schiff_base wikiPageWikiLink Aniline.
- Schiff_base wikiPageWikiLink Aromatic.
- Schiff_base wikiPageWikiLink Aromaticity.
- Schiff_base wikiPageWikiLink Asymmetric_catalysis.
- Schiff_base wikiPageWikiLink Carbonyl.
- Schiff_base wikiPageWikiLink Category:Functional_groups.
- Schiff_base wikiPageWikiLink Category:Imines.
- Schiff_base wikiPageWikiLink Coordination_chemistry.
- Schiff_base wikiPageWikiLink Coordination_complex.
- Schiff_base wikiPageWikiLink Coordination_complexes.
- Schiff_base wikiPageWikiLink Corrin.
- Schiff_base wikiPageWikiLink Covalent_organic_framework.
- Schiff_base wikiPageWikiLink Dehydration_reaction.
- Schiff_base wikiPageWikiLink Diamine.
- Schiff_base wikiPageWikiLink Electrochromic_devices.
- Schiff_base wikiPageWikiLink Enantioselective_synthesis.
- Schiff_base wikiPageWikiLink Fructose-bisphosphate_aldolase.
- Schiff_base wikiPageWikiLink Glycolysis.
- Schiff_base wikiPageWikiLink Hemiaminal.
- Schiff_base wikiPageWikiLink Hugo_Schiff.
- Schiff_base wikiPageWikiLink Imine.
- Schiff_base wikiPageWikiLink Imines.
- Schiff_base wikiPageWikiLink Intermolecular_metal-catalyzed_carbenoid_cyclopropanations.
- Schiff_base wikiPageWikiLink Jacobsens_catalyst.
- Schiff_base wikiPageWikiLink Ligand.
- Schiff_base wikiPageWikiLink Nobel_Prize_in_Chemistry.
- Schiff_base wikiPageWikiLink Nucleophilic_addition.
- Schiff_base wikiPageWikiLink Organic_field-effect_transistor.
- Schiff_base wikiPageWikiLink Organic_solar_cell.
- Schiff_base wikiPageWikiLink Perovskite_solar_cell.
- Schiff_base wikiPageWikiLink Phenyl.
- Schiff_base wikiPageWikiLink Phenyl_group.
- Schiff_base wikiPageWikiLink Pi_backbonding.
- Schiff_base wikiPageWikiLink Pyridoxal_phosphate.
- Schiff_base wikiPageWikiLink Retinal.
- Schiff_base wikiPageWikiLink Ryōji_Noyori.
- Schiff_base wikiPageWikiLink Salen_ligand.
- Schiff_base wikiPageWikiLink Salicylaldoxime.
- Schiff_base wikiPageWikiLink Styrene.
- Schiff_base wikiPageWikiLink Vanillin.
- Schiff_base wikiPageWikiLink File:Aldimine-(secondary)-skeletal.png.
- Schiff_base wikiPageWikiLink File:AsymmetricSynthesisNoyori.png.
- Schiff_base wikiPageWikiLink File:Imino_Group_V.1.png.
- Schiff_base wikiPageWikiLink File:Schiff_Base.png.
- Schiff_base wikiPageWikiLinkText "Schiff base linkage".
- Schiff_base wikiPageWikiLinkText "Schiff base reaction".
- Schiff_base wikiPageWikiLinkText "Schiff base".
- Schiff_base wikiPageWikiLinkText "Schiff reaction".
- Schiff_base wikiPageWikiLinkText "Schiff-base".
- Schiff_base wikiPageWikiLinkText "schiff base".
- Schiff_base wikiPageWikiLinkText "transchiffization".
- Schiff_base hasPhotoCollection Schiff_base.
- Schiff_base wikiPageUsesTemplate Template:Gallery.
- Schiff_base subject Category:Functional_groups.
- Schiff_base subject Category:Imines.
- Schiff_base hypernym Compound.
- Schiff_base type ChemicalCompound.
- Schiff_base type Group.
- Schiff_base type Group.
- Schiff_base comment "A Schiff base, named after Hugo Schiff, is a compound with the general structure R2C=NR' (R' ≠ H). They can be considered a sub-class of imines, being either secondary ketimines or secondary aldimines depending on their structure. The term is often synonymous with azomethine which refers specifically to secondary aldimines (i.e. RN=CR2 where R ≠ H).A number of special naming systems exist for these compounds.".
- Schiff_base label "Schiff base".
- Schiff_base sameAs قاعدة_شيف.
- Schiff_base sameAs Base_de_Schiff.
- Schiff_base sameAs شیفباز.
- Schiff_base sameAs Base_de_Schiff.
- Schiff_base sameAs シッフ塩基.
- Schiff_base sameAs Шифова_база.
- Schiff_base sameAs Schiff-base.
- Schiff_base sameAs Base_de_Schiff.
- Schiff_base sameAs m.02l5b2.
- Schiff_base sameAs Основания_Шиффа.
- Schiff_base sameAs Šifova_baza.
- Schiff_base sameAs Schiffova_baza.
- Schiff_base sameAs Šifova_baza.
- Schiff_base sameAs Основи_Шиффа.
- Schiff_base sameAs Q2602701.
- Schiff_base sameAs Q2602701.
- Schiff_base sameAs 希夫碱.
- Schiff_base wasDerivedFrom Schiff_base?oldid=682616094.
- Schiff_base depiction Imino_Group_V.1.png.
- Schiff_base isPrimaryTopicOf Schiff_base.