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Organic Electronics is a rapidly evolving multidisciplinary research field at the interface between Organic Chemistry and Physics. Organic Electronics is based on the use of the unique optical and electrical properties of π-conjugated materials that range from small molecules to polymers. The wide activity of researchers in Organic Electronics is testament to the fact that its potential is huge and its list of potential applications almost endless. Application of these electronic and optoelectronic devices range from Organic Field Effect Transistors (OFETs) to Organic Light Emitting Diodes (OLEDs) and Organic Solar Cells (OSCs), sensors, etc. We invited a series of colleagues to contribute to this Special Issue with respect to the aforementioned concepts and keywords. The goal for this Special Issue was to describe the recent developments of this rapidly advancing interdisciplinary research field. We thank all authors for their contributions.

Technology: general issues --- fluorene --- nitrofluorene --- Knoevenagel reaction --- near infrared absorption --- push–pull chromophore --- poly(nitro)fluorene --- organic tandem solar cell --- 3D nano-ripple pattern --- ZnO sol-gel --- charge recombination layer --- low temperature solution process --- on-surface reaction --- stepwise growth --- sequential growth --- hierarchical growth --- macromolecular organic structures --- surface covalent organic framework --- nanoribbons --- macrocycles --- coordination polymers --- silicon phthalocyanines --- n-type organic semiconductors --- organic thin-film transistors --- push-pull dyes --- chromophore --- naphthalene --- solvatochromism --- DFT --- fullerene derivative --- P3HT --- polymer solar cell --- QSPR --- TD-DFT

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Organic Electronics is a rapidly evolving multidisciplinary research field at the interface between Organic Chemistry and Physics. Organic Electronics is based on the use of the unique optical and electrical properties of π-conjugated materials that range from small molecules to polymers. The wide activity of researchers in Organic Electronics is testament to the fact that its potential is huge and its list of potential applications almost endless. Application of these electronic and optoelectronic devices range from Organic Field Effect Transistors (OFETs) to Organic Light Emitting Diodes (OLEDs) and Organic Solar Cells (OSCs), sensors, etc. We invited a series of colleagues to contribute to this Special Issue with respect to the aforementioned concepts and keywords. The goal for this Special Issue was to describe the recent developments of this rapidly advancing interdisciplinary research field. We thank all authors for their contributions.

fluorene --- nitrofluorene --- Knoevenagel reaction --- near infrared absorption --- push–pull chromophore --- poly(nitro)fluorene --- organic tandem solar cell --- 3D nano-ripple pattern --- ZnO sol-gel --- charge recombination layer --- low temperature solution process --- on-surface reaction --- stepwise growth --- sequential growth --- hierarchical growth --- macromolecular organic structures --- surface covalent organic framework --- nanoribbons --- macrocycles --- coordination polymers --- silicon phthalocyanines --- n-type organic semiconductors --- organic thin-film transistors --- push-pull dyes --- chromophore --- naphthalene --- solvatochromism --- DFT --- fullerene derivative --- P3HT --- polymer solar cell --- QSPR --- TD-DFT

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A compilation of papers presenting original research results in the areas of organic, inorganic, organometallic, solid state and theoretical chemistry with a common theme of the use of X-ray diffraction to solve chemical problems.

Research & information: general --- Chemistry --- Organic chemistry --- molecular magnetism --- supramolecular chemistry --- heterometallic clusters --- magnetometry --- EPR spectroscopy --- N-Substituted Benzamides --- Woollins’ reagent --- selenation reagent --- reduction reagent --- single crystal X-ray structures --- DFT --- 3d metal complex --- benchmark --- hydricity --- 2D Cu-MOF --- square grid structure --- Click reaction --- Knoevenagel reaction --- green chemistry --- titanium(IV) oxo-clusters --- band gap modification --- multinuclear NMR --- ESI-MS studies --- photoluminescence --- perophoramidine --- natural product --- Claisen rearrangement --- indoloquinoline --- intramolecular cyclization --- X-ray structure --- isothiourea --- ammonium enolate --- aryloxide --- quinone methide --- ester functionalization --- 1,6-conjugate addition --- layered perovskite --- bandgap tuning --- azetidinium --- Ruddlesden–Popper --- structure-property relations --- amide groups --- isomers --- late-transition metals --- P-ligands --- phenols --- secondary interactions --- single crystal X-ray crystallography --- MOF --- calcium MOF --- electrochemistry --- scXRD --- VTXRD --- bioMOF --- bond activation --- low oxidation state complexes --- magnesium --- metallacycles --- ring system --- X-ray crystallography --- peri-substitution --- arsenic --- organophosphorus --- pnictine --- PDS --- PELDOR --- DEER --- nitroxide spin label --- Comparative DEER Analyzer --- mtsslSuite --- MMM --- oxazoline --- Wittig rearrangement --- thiophene --- thieno[2,3-c]pyrrolone

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Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-coupling strategies, borrowing hydrogen catalysis, multicomponent and solvent-free reactions, regio- and stereoselective syntheses, as well as other new, attractive approaches for the construction of heterocyclic scaffolds are of great interest. This Special Issue is dedicated to featuring the latest research that is ongoing in the field of heterocyclic synthesis. It is expected that most submissions will focus on five- and six-membered oxygen and nitrogen-containing heterocycles, but structures incorporating other rings/heteroatoms will also be considered. Original research (communications, full papers and reviews) that discusses innovative methodologies for assembling heterocycles with potential application in materials, catalysis and medicine are therefore welcome.

Medicine --- amine nucleophiles --- alkynoic acids --- cascade reaction --- gold catalysis --- fused N-heterocycles --- solid-phase synthesis --- ketone --- traceless synthesis --- natural products --- enol ethers --- photocatalysis --- photoredox --- visible-light-induced catalysis --- photoredox cyclization --- organic dyes --- heterocycles --- dihydrocoumarins --- synthesis --- 3-trifluoroacetyl coumarins --- phenols --- antifungal activities --- terpyridines --- 3,2′:6′,3″-terpyridine --- cyclohexanol derivative --- condensation --- heterocyclic --- 1,2,3-triazol --- triazolylmethyl phosphinate --- triazolylmethyl phosphate --- copper-catalyzed azide-alkyne cycloaddition --- click reaction --- azides --- cinnolines --- triazoles --- CuAAC --- alkynes --- cycloalkynes --- Richter cyclization --- Suzuki coupling --- fluorescence --- cytotoxicity --- coumarin --- pyrazolo[3,4-b]pyridine --- silica sulfuric acid --- 2H-pyran --- valence isomerism --- 1-oxa-triene --- dienone --- oxa-electrocyclization --- Knoevenagel --- propargyl Claisen --- cycloisomerization --- asymmetric dimeric β-carboline --- acylhydrazone group --- cytotoxic --- antitumor --- structure–activity relationship --- γ-lactam --- pyrrolidones --- multicomponent reactions --- organocatalysis --- pyridine --- CF3CO-acetylenes --- 1,3-oxazines --- fluorinated heterocycles --- saturated oxygen heterocycles --- cyclic ethers --- total synthesis --- multicomponent reaction --- α-halohydrazones --- Staudinger reaction --- aza-Wittig --- 1H-imidazole-2(3H)-thione --- 2H-imidazo[2,1-b][1,3,4]thiadiazine --- purine --- nucleobase --- aromatic substitution --- arylation --- fluoroalcohol --- α-chloroglycinates --- 5-acylamino-1,3-thiazoles --- Hantzsch reaction --- TMSBr --- propargylic alcohols --- cascade cyclization --- 4-bromo quinolines --- synthesis of benzofurans --- intra-molecular approach --- inter-molecular approach --- n/a --- 3,2':6',3"-terpyridine --- structure-activity relationship

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Heterocycles feature widely in natural products, agrochemicals, pharmaceuticals and dyes, and their synthesis is of great interest to synthetic chemists in both academia and industry. The contributions of recent applications of new methodologies in C–H activation, photoredox chemistry, cross-coupling strategies, borrowing hydrogen catalysis, multicomponent and solvent-free reactions, regio- and stereoselective syntheses, as well as other new, attractive approaches for the construction of heterocyclic scaffolds are of great interest. This Special Issue is dedicated to featuring the latest research that is ongoing in the field of heterocyclic synthesis. It is expected that most submissions will focus on five- and six-membered oxygen and nitrogen-containing heterocycles, but structures incorporating other rings/heteroatoms will also be considered. Original research (communications, full papers and reviews) that discusses innovative methodologies for assembling heterocycles with potential application in materials, catalysis and medicine are therefore welcome.

amine nucleophiles --- alkynoic acids --- cascade reaction --- gold catalysis --- fused N-heterocycles --- solid-phase synthesis --- ketone --- traceless synthesis --- natural products --- enol ethers --- photocatalysis --- photoredox --- visible-light-induced catalysis --- photoredox cyclization --- organic dyes --- heterocycles --- dihydrocoumarins --- synthesis --- 3-trifluoroacetyl coumarins --- phenols --- antifungal activities --- terpyridines --- 3,2′:6′,3″-terpyridine --- cyclohexanol derivative --- condensation --- heterocyclic --- 1,2,3-triazol --- triazolylmethyl phosphinate --- triazolylmethyl phosphate --- copper-catalyzed azide-alkyne cycloaddition --- click reaction --- azides --- cinnolines --- triazoles --- CuAAC --- alkynes --- cycloalkynes --- Richter cyclization --- Suzuki coupling --- fluorescence --- cytotoxicity --- coumarin --- pyrazolo[3,4-b]pyridine --- silica sulfuric acid --- 2H-pyran --- valence isomerism --- 1-oxa-triene --- dienone --- oxa-electrocyclization --- Knoevenagel --- propargyl Claisen --- cycloisomerization --- asymmetric dimeric β-carboline --- acylhydrazone group --- cytotoxic --- antitumor --- structure–activity relationship --- γ-lactam --- pyrrolidones --- multicomponent reactions --- organocatalysis --- pyridine --- CF3CO-acetylenes --- 1,3-oxazines --- fluorinated heterocycles --- saturated oxygen heterocycles --- cyclic ethers --- total synthesis --- multicomponent reaction --- α-halohydrazones --- Staudinger reaction --- aza-Wittig --- 1H-imidazole-2(3H)-thione --- 2H-imidazo[2,1-b][1,3,4]thiadiazine --- purine --- nucleobase --- aromatic substitution --- arylation --- fluoroalcohol --- α-chloroglycinates --- 5-acylamino-1,3-thiazoles --- Hantzsch reaction --- TMSBr --- propargylic alcohols --- cascade cyclization --- 4-bromo quinolines --- synthesis of benzofurans --- intra-molecular approach --- inter-molecular approach --- n/a --- 3,2':6',3"-terpyridine --- structure-activity relationship