
Max Martin
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[ASAP] p-Extension of Strained Benzenoid Macrocycles Using the Scholl Reaction
Reductive diazotation of carbon nanotubes: an experimental and theoretical selectivity study
DOI: 10.1039/C8SC03737J, Edge Article
Open Access
  This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
The reaction of negatively charged SWCNTs with diazonium salts was analyzed in a combined experimental and computational DFT study.
The content of this RSS Feed (c) The Royal Society of Chemistry
[19]Dendriphene: A 19‐Ring Dendritic Nanographene
Nanographenes: The successful synthesis of a dendritic nanographene is reported. [19]Dendriphene, which is the largest unsubstituted cata‐condensed nanographene obtained by solution chemistry, was characterized on‐surface by scanning probe microscopy.
Abstract
The synthesis of a threefold symmetric nanographene with 19 cata‐fused benzene rings distributed within six branches is reported. This flat dendritic starphene, which is the largest unsubstituted cata‐condensed PAH that has been obtained to date, was prepared in solution by means of a palladium‐catalyzed aryne cyclotrimerization reaction and it was characterized on surface by scanning probe microscopy with atomic resolution.
Superbenzene–Porphyrin Gas‐Phase Architectures Derived from Intermolecular Dispersion Interactions
[ASAP] Fully Conjugated [4]Chrysaorene. Redox-Coupled Anion Binding in a Tetraradicaloid Macrocycle
Superoxide dismutase activity enabled by a redox-active ligand rather than metal
Superoxide dismutase activity enabled by a redox-active ligand rather than metal
Superoxide dismutase activity enabled by a redox-active ligand rather than metal, Published online: 01 October 2018; doi:10.1038/s41557-018-0137-1
Catalytic superoxide dismutase mimics typically involve manganese centres. Now, a complex based on redox-inactive zinc(ii) and a redox-active quinol ligand is found to catalytically degrade superoxide. The reaction, proposed to occur through oxidation of the ligand to a quinoxyl radical, is hastened rather than inhibited by the presence of phosphate.[ASAP] Concave–Convex p–p Template Approach Enables the Synthesis of [10]Cycloparaphenylene–Fullerene [2]Rotaxanes
Frontispiece: Fullerene Building Blocks with Tailor‐Made Solubility and New Insights into Their Hierarchical Self‐Assembly
Thiophene and its sulfur inhibit indenoindenodibenzothiophene diradicals from low-energy lying thermal triplets
Thiophene and its sulfur inhibit indenoindenodibenzothiophene diradicals from low-energy lying thermal triplets
Thiophene and its sulfur inhibit indenoindenodibenzothiophene diradicals from low-energy lying thermal triplets, Published online: 17 September 2018; doi:10.1038/s41557-018-0133-5
A paradoxical case of a well-defined diradicaloid that has an unusually large singlet–triplet energy gap (ΔES-T) imparted by the thiophene sulfur atom is reported. Quantum chemistry, organic synthesis, molecular spectroscopies, X-ray crystal analysis and high-temperature magnetic measurements help account for the dichotomy between the large diradical character and large ΔEST.Binary supramolecular networks of bridged triphenylamines with different substituents and identical scaffolds
DOI: 10.1039/C8CC04410D, Communication
Based on scanning tunneling microscopy experiments combined with density functional theory, we report the formation and the electronic structure of porous binary supramolecular networks on Au(111).
The content of this RSS Feed (c) The Royal Society of Chemistry
[ASAP] Porous Shape-Persistent Organic Cage Compounds of Different Size, Geometry, and Function
Gram‐Scale Synthesis of a C2v‐Symmetric Hexaphenylbenzene with Three Different Types of Substituents
A large‐scale selective synthesis of a C 2v‐symmetric hexaphenylbenzene (HPB) derivative with three kinds of substituents on the periphery of HPB was realized using inexpensive reagents.
Abstract
A large‐scale selective synthesis of a C 2v‐symmetric hexaphenylbenzene (HPB) derivative with three different kinds of substituents on the periphery of HPB was realized using inexpensive reagents. All the reactions were carried out at room temperature or by heating and most materials along the synthetic route could be isolated without chromatographic purification.
[ASAP] Template-Directed Synthesis of Molecular Nanorings and Cages
Superbenzene–Porphyrin Gas‐Phase Architectures Derived from Intermolecular Dispersion Interactions
[ASAP] Ruthenium(II)-Catalyzed Microwave-Promoted Multiple C–H Activation in Synthesis of Hexa(heteroaryl)benzenes in Water
Oxo‐Functionalized Graphene: A Versatile Precursor for Alkylated Graphene Sheets by Reductive Functionalization
A Tethered Tolane: Twisting the Excited State
[ASAP] Intrinsic Properties of Single Graphene Nanoribbons in Solution: Synthetic and Spectroscopic Studies
Topological band engineering of graphene nanoribbons
Topological band engineering of graphene nanoribbons
Topological band engineering of graphene nanoribbons, Published online: 08 August 2018; doi:10.1038/s41586-018-0376-8
A topologically engineered graphene nanoribbon superlattice is presented that hosts a one-dimensional array of half-filled, in-gap localized electronic states, enabling band engineering.Engineering of robust topological quantum phases in graphene nanoribbons
Engineering of robust topological quantum phases in graphene nanoribbons
Engineering of robust topological quantum phases in graphene nanoribbons, Published online: 08 August 2018; doi:10.1038/s41586-018-0375-9
Graphene nanoribbons are used to design robust nanomaterials with controlled periodic coupling of topological boundary states to create quasi-one-dimensional trivial and non-trivial electronic quantum phases.Fullerene Building Blocks with Tailor‐Made Solubility and New Insights into Their Hierarchical Self‐Assembly
[ASAP] Synthesis and Size-Dependent Properties of [12], [16], and [24]Carbon Nanobelts
[ASAP] Bottom-Up Synthesis of Heteroatom-Doped Chiral Graphene Nanoribbons
Highly Efficient Encapsulation and Phase Separation of Apolar Molecules by Magnetic Shell‐by‐Shell‐Coated Nanocarriers in Water
A Phenylene‐Bridged Cyclohexa‐meta‐phenylene as Hexa‐peri‐hexabenzocoronene Precursor
Bonding and Mobility of Alkali Metals in Helicenes
Interfacing porphyrins and carbon nanotubes through mechanical links
DOI: 10.1039/C8SC02492H, Edge Article
Open Access
  This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
U-shaped bisporphyrin molecules are clipped around SWCNTs using ring-closing metathesis yielding rotaxane-type derivatives, in which porphyrins and SWCNTs are connected through mechanical links.
The content of this RSS Feed (c) The Royal Society of Chemistry
Hexakis(3,6‐di‐tert‐butyl‐4‐oxo‐2,5‐cyclohexadien‐1‐ylidene)cyclohexane: Closed‐Shell [6]Radialene or Open‐Shell Hexa‐Radicaloid?
Triply Linked Porphyrinoids
The best things come in threes: Triply linked porphyrin arrays, so called porphyrin tapes, are intriguing molecules in terms of their stability, far red‐shifted absorption band, multi‐charge storage ability, and conductivity. Recent advances in the chemistry of porphyrin tape are summarized in this Minireview, in particular, the development of porphyrin tape variants such as expanded porphyrin hybrid tape, porphyrin arch‐tape, corrole tape, and subporphyrin tape.
Abstract
Triply linked porphyrin arrays, so called porphyrin tapes, are intriguing molecules in terms of their planar structures, far red‐shifted absorption bands, multi‐charge storage abilities, and high conductivities. Recently, porphyrin tape variants such as porphyrin‐expanded porphyrin hybrid tapes, porphyrin arch‐tapes, corrole tapes, and a subporphyrin tape have been explored as novel π‐conjugated materials. These new molecules exhibit electronic and structural characteristics owing to direct triple linkages. This Minireview first discusses the fundamental properties of the parent porphyrin tapes and the peripherally functionalized porphyrin tapes. Then, a focus has been placed on the syntheses, structures, and unique properties of the recently explored porphyrin tape variants.








