All Stories

  1. Trialkoxysilane Grafting in Alcohols: A Simple Approach towards Modified Silica-Based Materials
  2. Easy functionalization of carbon nano-onions with disulfides and their use as recyclable heterogeneous organocatalysts
  3. Polymerizable deep eutectic solvents: Convenient reactive dispersion media for the preparation of novel multi-walled carbon nanotubes-based functional materials
  4. Phosphonium Salt/Al‐Porphyrin Copolymer as Bifunctional Heterogeneous Catalyst for CO2 Conversion to Cyclic Carbonates
  5. Highly cross-linked bifunctional magnesium porphyrin-imidazolium bromide polymer: Unveiling the key role of co-catalysts proximity for CO2 conversion into cyclic carbonates
  6. A Prato Tour on Carbon Nanotubes: Raman Insights
  7. Highly Functionalized SWCNTs with a Dopamine Derivative as a Support for Pd Nanoparticles: A Recyclable Catalyst for the Reduction of Nitro Compounds and the Heck Reaction
  8. POSS-Al-porphyrin-imidazolium cross-linked network as catalytic bifunctional platform for the conversion of CO2 with epoxides
  9. Air-stable ternary organic solar cells achieved by using fullerene additives in non-fullerene acceptor-polymer donor blends
  10. Enhanced Conversion of Carbon Dioxide Promoted by Highly Cross-Linked Bifunctional Polymer: Unveiling the Key Role of Co-Catalysts Proximity
  11. Front Cover: Catechol‐Functionalized Carbon Nanotubes as Support for Pd Nanoparticles: a Recyclable System for the Heck Reaction (Eur. J. Org. Chem. 45/2022)
  12. Heterogenizing palladium tetraiodide catalyst for carbonylation reactions
  13. Is a Catalyst Always Needed? The Case of the Knoevenagel Reaction with Malononitrile
  14. Is a Catalyst Always Needed? The Case of the Knoevenagel Reaction with Malononitrile
  15. Catechol‐Functionalized Carbon Nanotubes as Support for Pd Nanoparticles: a Recyclable System for the Heck Reaction
  16. New biocides based on imidazolinium-functionalised hybrid mesoporous silica nanoparticles
  17. Supported Poly(Ionic Liquid)-Heteropolyacid Based Materials for Heterogeneous Catalytic Fructose Dehydration in Aqueous Medium
  18. Low Angle Bending Detection Semi-transparent Piezoresistive Sensor
  19. First Evidence of Tris(catecholato)silicate Formation from Hydrolysis of an Alkyl Bis(catecholato)silicate
  20. Carbon nanotube supported aluminum porphyrin-imidazolium bromide crosslinked copolymer: A synergistic bifunctional catalyst for CO2 conversion
  21. White light emitting silsesquioxane based materials: the importance of a ligand with rigid and directional arms
  22. Heterogenizing Palladium Tetraiodide Catalyst for Carbonylation Reactions
  23. Poss-Al-Porphyrin-Imidazolium Cross-Linked Network as Catalytic Bifunctional Platform for the Conversion of Co2 with Epoxides
  24. New Hybrid Organic‐inorganic Multifunctional Materials Based on Polydopamine‐like Chemistry
  25. A Study on the Stability of Carbon Nanoforms–Polyimidazolium Network Hybrids in the Conversion of CO2 into Cyclic Carbonates: Increase in Catalytic Activity after Reuse
  26. Bending Sensors Based on Thin Films of Semitransparent Bithiophene‐Fulleropyrrolidine Bisadducts
  27. Reconsidering TOF calculation in the transformation of epoxides and CO2 into cyclic carbonates
  28. Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self‐Assemble in the Presence of Europium(III) Ions: Reversible trans ‐to‐ cis Isomerization
  29. Straightforward preparation of highly loaded MWCNT–polyamine hybrids and their application in catalysis
  30. POSS nanostructures in catalysis
  31. Tuneable Emission of Polyhedral Oligomeric Silsesquioxane Based Nanostructures that Self‐Assemble in the Presence of Europium(III) Ions: Reversible trans ‐to‐ cis Isomerization
  32. Efficient Conversion of Carbon Dioxide by Imidazolium‐Based Cross‐Linked Nanostructures Containing Polyhedral Oligomeric Silsesquioxane (POSS) Building Blocks
  33. SBA‐15/POSS‐Imidazolium Hybrid as Catalytic Nanoreactor: the role of the Support in the Stabilization of Palladium Species for C−C Cross Coupling Reactions.
  34. Templating effect of carbon nanoforms on highly cross‐linked imidazolium network: Catalytic activity of the resulting hybrids with Pd nanoparticles
  35. Hybrid Catalysts for CO2 Conversion into Cyclic Carbonates
  36. Supported Polyhedral Oligomeric Silsesquioxane‐Based (POSS) Materials as Highly Active Organocatalysts for the Conversion of CO 2
  37. Modified Nanocarbons for Catalysis
  38. Cross-Linked Polyamine from Imidazolium-Based Materials: A Simple Route to Useful Catalytic Materials
  39. Enhanced power-conversion efficiency in organic solar cells incorporating copolymeric phase-separation modulators
  40. Supported Ionic Liquids: A Versatile and Useful Class of Materials
  41. Correction: Supported C60-IL-PdNPs as extremely active nanocatalysts for C–C cross-coupling reactions
  42. Imidazolium-Functionalized Carbon Nanohorns for the Conversion of Carbon Dioxide: Unprecedented Increase of Catalytic Activity after Recycling
  43. DNA-Binding and Anticancer Activity of Pyrene-Imidazolium Derivatives
  44. Sensor Properties of Pristine and Functionalized Carbon Nanohorns
  45. Advances in Organic and Organic-Inorganic Hybrid Polymeric Supports for Catalytic Applications
  46. Single-Walled Carbon Nanotube–Polyamidoamine Dendrimer Hybrids for Heterogeneous Catalysis
  47. Proximity Effect using a Nanocage Structure: Polyhedral Oligomeric Silsesquioxane-Imidazolium Tetrachloro- palladate Salt as a Precatalyst for the Suzuki-Miyaura Reaction in Water
  48. Highly Loaded Multi-Walled Carbon Nanotubes Non-Covalently Modified with a Bis-Imidazolium Salt and their Use as Catalyst Supports
  49. ChemInform Abstract: Covalently Supported Ionic Liquid Phases: An Advanced Class of Recyclable Catalytic Systems
  50. Covalently Supported Ionic Liquid Phases: An Advanced Class of Recyclable Catalytic Systems
  51. Supported C60-IL-PdNPs as extremely active nanocatalysts for C–C cross-coupling reactions
  52. ChemInform Abstract: A Simple Procedure for the Oxidation of Alcohols Using [Bis(acetoxy)iodo]benzene and a Catalytic Amount of Bromide Ions in Ethyl Acetate.
  53. Cross-Linked Thiazolidine Network as Support for Palladium: A New Catalyst for Suzuki and Heck Reactions
  54. A Simple Procedure for the Oxidation of Alcohols Using [Bis(acetoxy)iodo]benzene and a Catalytic Amount of Bromide Ions in Ethyl Acetate
  55. Thiazolium-Based Catalysts for the Etherification of Benzylic Alcohols under Solvent-Free Conditions
  56. Extremely water-soluble fullerenes
  57. Carbon Nanoforms can be easily functionalized with disulfides, diselenides and ditellurides
  58. A polyhedral oligomeric silsesquioxane-based catalyst for the efficient synthesis of cyclic carbonates
  59. Catalytic Synergism in a C60IL10TEMPO2Hybrid in the Efficient Oxidation of Alcohols
  60. Efficient microwave-mediated synthesis of fullerene acceptors for organic photovoltaics
  61. An E-Factor Minimized Protocol for a Sustainable and Efficient Heck Reaction in Flow
  62. Highly selective detection of Epinephrine at oxidized Single-Wall Carbon Nanohorns modified Screen Printed Electrodes (SPEs)
  63. Fullerene as a Platform for Recyclable TEMPO Organocatalysts for the Oxidation of Alcohols
  64. Evidences of release and catch mechanism in the Heck reaction catalyzed by palladium immobilized on highly cross-linked-supported imidazolium salts
  65. Recyclable Heterogeneous and Low‐Loading Homogeneous Chiral Imidazolidinone Catalysts for α‐Alkylation of Aldehydes
  66. ChemInform Abstract: Non‐Conventional Methods and Media for the Activation and Manipulation of Carbon Nanoforms
  67. ChemInform Abstract: Recyclable Catalyst Reservoir: Oxidation of Alcohols Mediated by Noncovalently Supported Bis(imidazolium)‐Tagged 2,2,6,6‐Tetramethylpiperidine 1‐Oxyl.
  68. Cross‐Linked Imidazolium Salts as Scavengers for Palladium
  69. Non-conventional methods and media for the activation and manipulation of carbon nanoforms
  70. ChemInform Abstract: Palladium Supported on Cross‐Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions.
  71. ChemInform Abstract: “Release and Catch” Catalytic Systems
  72. Water in Organocatalytic Reactions
  73. Palladium Supported on Cross‐Linked Imidazolium Network on Silica as Highly Sustainable Catalysts for the Suzuki Reaction under Flow Conditions
  74. Recyclable Catalyst Reservoir: Oxidation of Alcohols Mediated by Noncovalently Supported Bis(imidazolium)‐Tagged 2,2,6,6‐Tetramethylpiperidine 1‐Oxyl
  75. An Atom‐Economical Approach to Functionalized Single‐Walled Carbon Nanotubes: Reaction with Disulfides
  76. An Atom‐Economical Approach to Functionalized Single‐Walled Carbon Nanotubes: Reaction with Disulfides
  77. ChemInform Abstract: “Nonsolvent” Applications of Ionic Liquids in Organocatalysis
  78. “Release and catch” catalytic systems
  79. Buckyballs
  80. ChemInform Abstract: A Liquid—Liquid Biphasic Homogeneous Organocatalytic Aldol Protocol Based on the Use of a Silica Gel Bound Multilayered Ionic Liquid Phase.
  81. ChemInform Abstract: Hydrogen Bonding Donor‐Acceptor Carbon Nanostructures
  82. ChemInform Abstract: Low‐Loading Asymmetric Organocatalysis
  83. A Straightforward Electroactive π‐Extended Tetrathiafulvalene (exTTF) Building Block
  84. A Liquid–Liquid Biphasic Homogeneous Organocatalytic Aldol Protocol Based on the Use of a Silica Gel Bound Multilayered Ionic Liquid Phase
  85. Carbon Nanostructures: Covalent and Macromolecular Chemistry
  86. ChemInform Abstract: Asymmetric Synthesis Using Polymer‐Immobilized Proline Derivatives
  87. “Nonsolvent” Applications of Ionic Liquids in Organocatalysis
  88. Low-loading asymmetric organocatalysis
  89. Multilayered Supported Ionic Liquids as Catalysts for Chemical Fixation of Carbon Dioxide: A High‐Throughput Study in Supercritical Conditions
  90. Polystyrene-supported organocatalysts for α-selenenylation and Michael reactions
  91. Multi‐Layered, Covalently Supported Ionic Liquid Phase (mlc‐SILP) as Highly Cross‐Linked Support for Recyclable Palladium Catalysts for the Suzuki Reaction in Aqueous Medium
  92. Catalytic Methods in Asymmetric Synthesis
  93. Recyclable Organocatalysts in Asymmetric Reactions
  94. Asymmetric Synthesis Using Polymer‐Immobilized Proline Derivatives
  95. ChemInform Abstract: Supported Organocatalysts as a Powerful Tool in Organic Synthesis
  96. Chapter 4. Fullerene-Containing Polymers
  97. Chapter 6. Hydrogen Bonding Donor–Acceptor Carbon Nanostructures
  98. New Concepts and Applications in the Macromolecular Chemistry of Fullerenes
  99. Advances towards Highly Active and Stereoselective Simple and Cheap Proline‐Based Organocatalysts
  100. Supported Organocatalysts as a Powerful Tool in Organic Synthesis
  101. ChemInform Abstract: Enhanced Activity and Stereoselectivity of Polystyrene‐Supported Proline‐Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water.
  102. Asymmetric Aldol Reaction with Polystyrene-Supported Proline-Based Catalysts
  103. Enhanced Activity and Stereoselectivity of Polystyrene‐Supported Proline‐Based Organic Catalysts for Direct Asymmetric Aldol Reaction in Water
  104. Fullerene Polymers
  105. Fullerene‐Containing Polymers: An Overview
  106. Main‐Chain and Side‐Chain C 60 ‐Polymers
  107. ChemInform Abstract: Water in Stereoselective Organocatalytic Reactions
  108. ChemInform Abstract: New Simple Hydrophobic Proline Derivatives as Highly Active and Stereoselective Catalysts for the Direct Asymmetric Aldol Reaction in Aqueous Medium.
  109. Water in Stereoselective Organocatalytic Reactions
  110. New Simple Hydrophobic Proline Derivatives as Highly Active and Stereoselective Catalysts for the Direct Asymmetric Aldol Reaction in Aqueous Medium
  111. ChemInform Abstract: Supported Proline and Proline‐Derivatives as Recyclable Organocatalysts
  112. ChemInform Abstract: Novel Prolinamide‐Supported Polystyrene as Highly Stereoselective and Recyclable Organocatalyst for the Aldol Reaction.
  113. Direct Asymmetric Aldol Reaction Using Polystyrene-Supported Proline Amide
  114. ChemInform Abstract: First Evidence of Proline Acting as a Bifunctional Catalyst in the Baylis—Hillman Reaction Between Alkyl Vinyl Ketones and Aryl Aldehydes.
  115. Novel Prolinamide‐Supported Polystyrene as Highly Stereoselective and Recyclable Organocatalyst for the Aldol Reaction
  116. ChemInform Abstract: New Ionic Liquid‐Modified Silica Gels as Recyclable Materials for L‐Proline‐ or H—Pro—Pro—Asp—NH2‐Catalyzed Aldol Reaction.
  117. Polystyrene-supported proline as recyclable catalyst in the Baylis–Hillman reaction of arylaldehydes and methyl or ethyl vinyl ketone
  118. First Evidence of Proline Acting as a Bifunctional Catalyst in the Baylis–Hillman Reaction Between Alkyl Vinyl Ketones and Aryl Aldehydes
  119. ChemInform Abstract: Hydrophobically Directed Aldol Reactions: Polystyrene‐Supported L‐Proline as a Recyclable Catalyst for Direct Asymmetric Aldol Reactions in the Presence of Water.
  120. Supported proline and proline-derivatives as recyclable organocatalysts
  121. Heterogeneous Catalytic Asymmetric Direct Aldol Reaction in Water
  122. Fullerene Polymers: Synthetic Strategies, Properties and Applications
  123. Hydrophobically Directed Aldol Reactions: Polystyrene‐Supported L‐Proline as a Recyclable Catalyst for Direct Asymmetric Aldol Reactions in the Presence of Water
  124. Hydrophobically Directed Aldol Reactions: Polystyrene‐Supported L‐Proline as a Recyclable Catalyst for Direct Asymmetric Aldol Reactions in the Presence of Water (Eur. J. Org. Chem. 28/2007)
  125. Fullerene Polymers: Synthesis and Properties
  126. Polystyrene‐Supported Proline and Prolinamide. Versatile Heterogeneous Organocatalysts Both for Asymmetric Aldol Reaction in Water and α‐Selenenylation of Aldehydes.
  127. Asymmetric Aldol Reaction in Water Catalyzed by Polystyrene-Supported Proline
  128. Chapter 6. Hydrogen Bonding Donor–Acceptor Carbon Nanostructures
  129. Polystyrene-supported proline and prolinamide. Versatile heterogeneous organocatalysts both for asymmetric aldol reaction in water and α-selenenylation of aldehydes
  130. Tetrathiafulvalene-based molecular nanowires
  131. New ionic liquid-modified silica gels as recyclable materials for l-proline- or H–Pro–Pro–Asp–NH2-catalyzed aldol reaction
  132. Cyclodextrin‐[6]fullerene Conjugates: Synthesis, Characterization, and Electrochemical Behavior.
  133. Fullerene Polymers:  Synthesis and Properties
  134. Cyclodextrin-[60]fullerene conjugates: synthesis, characterization, and electrochemical behavior
  135. Lipase-catalyzed resolution of anti-6-substituted 1,3-dioxepan-5-ols
  136. Long-Lived Photoinduced Charges in Donor−Acceptor Anthraquinone-Substituted Thiophene Copolymers
  137. Solid Film versus Solution‐Phase Charge‐Recombination Dynamics of exTTF–Bridge–C60 Dyads
  138. Topological Effects of a Rigid Chiral Spacer on the Electronic Interactions in Donor–Acceptor Ensembles
  139. Design, synthesis and photovoltaic properties of [60]fullerene based molecular materials
  140. Diphenylmethanofullerenes: New and Efficient Acceptors in Bulk-Heterojunction Solar Cells
  141. Cover Picture: Probing Molecular Wires: Synthesis, Structural, and Electronic Study of Donor–Acceptor Assemblies Exhibiting Long‐Range Electron Transfer (Chem. Eur. J. 16/2005)
  142. Probing Molecular Wires: Synthesis, Structural, and Electronic Study of Donor–Acceptor Assemblies Exhibiting Long‐Range Electron Transfer
  143. Concentration dependence of amplified spontaneous emission in two oligo-(p-phenylenevinylene) derivatives
  144. Electronic Communication through π‐Conjugated Wires in Covalently Linked Porphyrin/C60 Ensembles
  145. Mimicking photosynthesis: covalent [60]fullerene-based donor–acceptor ensembles
  146. Exceptionally Small Attenuation Factors in Molecular Wires
  147. Polymer solar cells with novel fullerene-based acceptor
  148. Donor?acceptor ?double-cable? polythiophenes with tunable acceptor content
  149. Tuning of the photoinduced charge transfer process in donor-acceptor double-cable copolymers
  150. Donor–acceptor polythiophene copolymers with tunable acceptor content for photoelectric conversion devices
  151. Tuning of the photoinduced charge transfer process in donor–acceptor double-cable copolymers
  152. Synthesis and Photoluminescent Properties of 1,1′‐Binaphthyl‐Based Chiral Phenylenevinylene Dendrimers.
  153. Synthesis of Soluble Donor−Acceptor Double-Cable Polymers Based on Polythiophene and Tetracyanoanthraquinodimethane (TCAQ)
  154. Synthesis and Photoluminescent Properties of 1,1‘-Binaphthyl-Based Chiral Phenylenevinylene Dendrimers
  155. ChemInform Abstract: Synthesis of 1,1′‐Binaphthyl‐Based Enantiopure C60 Dimers.
  156. Synthesis of 1,1‘-Binaphthyl-Based Enantiopure C60 Dimers