Nature Chemistry, ISSN 1755-4330, 07/2013, Volume 5, Issue 7, pp. 572 - 576
Carbon nanotubes (CNTs), tubular molecular entities that consist of sp(2)-hybridized carbon atoms, are currently produced as mixtures that contain tubes of...
RECOGNITION | SELECTIVE SYNTHESIS | CHEMICAL-SYNTHESIS | STEP | SEPARATION | CATALYST | CHIRALITY | CHEMISTRY, MULTIDISCIPLINARY | BOTTOM-UP SYNTHESIS | Spectrometry, Fluorescence | Spectrum Analysis, Raman | Spectrophotometry, Infrared | Nanotubes, Carbon | Stereoisomerism
RECOGNITION | SELECTIVE SYNTHESIS | CHEMICAL-SYNTHESIS | STEP | SEPARATION | CATALYST | CHIRALITY | CHEMISTRY, MULTIDISCIPLINARY | BOTTOM-UP SYNTHESIS | Spectrometry, Fluorescence | Spectrum Analysis, Raman | Spectrophotometry, Infrared | Nanotubes, Carbon | Stereoisomerism
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 2009, Volume 48, Issue 33, pp. 6112 - 6116
Journal Article
Accounts of Chemical Research, ISSN 0001-4842, 08/2012, Volume 45, Issue 8, pp. 1378 - 1389
Since their discovery in 1991, carbon nanotubes (CNTs) have attracted significant attention because of their remarkable mechanical, electronic, and optical...
CROSS-COUPLING REACTIONS | MECHANISM | CRYSTAL-STRUCTURE | GROWTH | CHEMICAL-SYNTHESIS | CHIRALITY | TRANSPARENT | CHEMISTRY, MULTIDISCIPLINARY | TETRADEHYDRODIANTHRACENE | BOTTOM-UP SYNTHESIS | Nanotechnology - methods | Nanotubes, Carbon - chemistry | Stereoisomerism | Benzene - chemical synthesis | Benzene - chemistry | Crystallography, X-Ray | Chemistry Techniques, Synthetic - methods | Analysis | Nanotubes | Chemical bonds | Ring formation (Chemistry) | Chemical properties | Structure | Chemical vapor deposition | Purification | Synthesis | Chairs | Arc discharges | Carbon nanotubes | Electronics | Nanostructure | Carbon
CROSS-COUPLING REACTIONS | MECHANISM | CRYSTAL-STRUCTURE | GROWTH | CHEMICAL-SYNTHESIS | CHIRALITY | TRANSPARENT | CHEMISTRY, MULTIDISCIPLINARY | TETRADEHYDRODIANTHRACENE | BOTTOM-UP SYNTHESIS | Nanotechnology - methods | Nanotubes, Carbon - chemistry | Stereoisomerism | Benzene - chemical synthesis | Benzene - chemistry | Crystallography, X-Ray | Chemistry Techniques, Synthetic - methods | Analysis | Nanotubes | Chemical bonds | Ring formation (Chemistry) | Chemical properties | Structure | Chemical vapor deposition | Purification | Synthesis | Chairs | Arc discharges | Carbon nanotubes | Electronics | Nanostructure | Carbon
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2011, Volume 50, Issue 14, pp. 3244 - 3248
Crystal clear: The title macrocycle was constructed by a nickel‐mediated shotgun macrocyclization. The X‐ray crystallographic structure of [12]CPP revealed a...
x‐ray crystal structures | nanotubes | nickel | macrocycles | cycloparaphenylenes | x-ray crystal structures | COMPLEXES | BIARYL SYNTHESIS | ELIMINATION | ZEROVALENT NICKEL | CHEMISTRY, MULTIDISCIPLINARY | CARBON NANOTUBES | SHAPE-PERSISTENT | COUPLING REACTIONS | ARYL HALIDES | SELECTIVE SYNTHESIS
x‐ray crystal structures | nanotubes | nickel | macrocycles | cycloparaphenylenes | x-ray crystal structures | COMPLEXES | BIARYL SYNTHESIS | ELIMINATION | ZEROVALENT NICKEL | CHEMISTRY, MULTIDISCIPLINARY | CARBON NANOTUBES | SHAPE-PERSISTENT | COUPLING REACTIONS | ARYL HALIDES | SELECTIVE SYNTHESIS
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2014, Volume 53, Issue 12, pp. 3102 - 3106
A new strategy for the non‐chromatographic extraction of metallofullerenes from solutions of arc‐processed raw soot is based on the size‐selective complexation...
host–guest systems | macrocycles | conjugation | metallofullerenes | cycloparaphenylenes | host-guest systems | CRYSTAL-STRUCTURE | SPECTROSCOPIC PROPERTIES | STEP | CHEMISTRY, MULTIDISCIPLINARY | CARBON NANOTUBES | NANORINGS | DEPENDENCE | FULLERENES | PURIFICATION | SEPARATION | BOTTOM-UP SYNTHESIS | Stereoisomerism | Molecular Structure | Fullerenes - chemistry | Chromatography | Complexation | Soot | Metallofullerenes | Fullerenes | Strategy | Raw | Affinity | Extraction
host–guest systems | macrocycles | conjugation | metallofullerenes | cycloparaphenylenes | host-guest systems | CRYSTAL-STRUCTURE | SPECTROSCOPIC PROPERTIES | STEP | CHEMISTRY, MULTIDISCIPLINARY | CARBON NANOTUBES | NANORINGS | DEPENDENCE | FULLERENES | PURIFICATION | SEPARATION | BOTTOM-UP SYNTHESIS | Stereoisomerism | Molecular Structure | Fullerenes - chemistry | Chromatography | Complexation | Soot | Metallofullerenes | Fullerenes | Strategy | Raw | Affinity | Extraction
Journal Article
Applied Physics Express, ISSN 1882-0778, 01/2020, Volume 13, Issue 1, p. 15002
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2010, Volume 49, Issue 52, pp. 10202 - 10205
A modular strategy served in the size‐selective syntheses of [14]‐, [15]‐, and [16]cycloparaphenylenes (CPPs). A Suzuki–Miyaura coupling was used to assemble a...
nanotubes | cross‐coupling | macrocycles | cycloparaphenylenes | cross-coupling | PORPHYRIN | CHEMISTRY, MULTIDISCIPLINARY | NONPLANAR AROMATIC-COMPOUNDS | BELT | GROWTH | PI-SYSTEMS | C-60 | CHIRALITY | TETRADEHYDRODIANTHRACENE
nanotubes | cross‐coupling | macrocycles | cycloparaphenylenes | cross-coupling | PORPHYRIN | CHEMISTRY, MULTIDISCIPLINARY | NONPLANAR AROMATIC-COMPOUNDS | BELT | GROWTH | PI-SYSTEMS | C-60 | CHIRALITY | TETRADEHYDRODIANTHRACENE
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2016, Volume 55, Issue 1, pp. 199 - 202
D5h‐symmetric fullerene C70 (D5h‐C70) is one of the most abundant members of the fullerene family. One longstanding mystery in the field of fullerene chemistry...
density functional calculations | X‐ray diffraction | lanthanum | metallofullerenes | electronic structure | X-ray diffraction | Rare earth metals
density functional calculations | X‐ray diffraction | lanthanum | metallofullerenes | electronic structure | X-ray diffraction | Rare earth metals
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2009, Volume 48, Issue 33, pp. 6112 - 6116
Tighten your belt: [12]Cycloparaphenylene, the sidewall segment of a carbon nanotube (see picture), has been synthesized in a selective manner through stepwise...
palladium | macrocyclization | cross‐coupling | aromaticity | cycloparaphenylenes | ORGANOBORON COMPOUNDS | TUBE-SHAPED MOLECULES | CARBON SKELETON | DOUBLE-STRANDED CYCLE | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | CROSS-COUPLING REACTIONS | NONPLANAR AROMATIC-COMPOUNDS | cross-coupling | H BOND ARYLATION | PI-SYSTEMS | BELT REGION
palladium | macrocyclization | cross‐coupling | aromaticity | cycloparaphenylenes | ORGANOBORON COMPOUNDS | TUBE-SHAPED MOLECULES | CARBON SKELETON | DOUBLE-STRANDED CYCLE | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | CROSS-COUPLING REACTIONS | NONPLANAR AROMATIC-COMPOUNDS | cross-coupling | H BOND ARYLATION | PI-SYSTEMS | BELT REGION
Journal Article
Organic Letters, ISSN 1523-7060, 05/2010, Volume 12, Issue 10, pp. 2262 - 2265
The structures and strain energies of cycloparaphenylenes (CPPs) have been determined by DFT calculation at the B3LYP/6-31G(d) level of theory. Fifteen stable...
CONJUGATED SYSTEMS | HYDROCARBONS | CHEMISTRY, ORGANIC | BELTS | BOND | CARBON NANOTUBES | TETRADEHYDRODIANTHRACENE | Thermodynamics | Molecular Structure | Models, Chemical | Benzene Derivatives - chemistry | Computer Simulation
CONJUGATED SYSTEMS | HYDROCARBONS | CHEMISTRY, ORGANIC | BELTS | BOND | CARBON NANOTUBES | TETRADEHYDRODIANTHRACENE | Thermodynamics | Molecular Structure | Models, Chemical | Benzene Derivatives - chemistry | Computer Simulation
Journal Article
Molecules, ISSN 1420-3049, 05/2017, Volume 22, Issue 5, p. 718
The purification of endohedral metallofullerenes by high performance liquid chromatography is very time-consuming and expensive. A number of rapid and...
Fullerene | Lewis acid | Complexation | Cycloparapheneylene | Metallofullerene | FILTER APPROACH | metallofullerene | HPLC PURIFICATION | CHEMISTRY, ORGANIC | STRUCTURAL-CHARACTERIZATION | CHEMICAL OXIDATION | CARBON NANOTUBES | SELECTIVE COMPLEXATION | EXTRACTION | lewis acid | METALLIC NITRIDE FULLERENES | CRYSTALLOGRAPHIC CHARACTERIZATION | cycloparapheneylene | complexation | fullerene | MRI CONTRAST AGENTS | Lewis Acids - chemistry | Fullerenes - isolation & purification | Organosilicon Compounds - chemistry | Oxidation-Reduction | Chromatography, High Pressure Liquid | Fullerenes - chemistry | Photochemical Processes | Separation | Purification | Metallofullerenes | Liquid chromatography | High-performance liquid chromatography | Chromatography | Electrode potentials | Reduction (metal working) | Efficiency | Fullerenes | Electrochemistry | Oxidation | Methods | High performance liquid chromatography
Fullerene | Lewis acid | Complexation | Cycloparapheneylene | Metallofullerene | FILTER APPROACH | metallofullerene | HPLC PURIFICATION | CHEMISTRY, ORGANIC | STRUCTURAL-CHARACTERIZATION | CHEMICAL OXIDATION | CARBON NANOTUBES | SELECTIVE COMPLEXATION | EXTRACTION | lewis acid | METALLIC NITRIDE FULLERENES | CRYSTALLOGRAPHIC CHARACTERIZATION | cycloparapheneylene | complexation | fullerene | MRI CONTRAST AGENTS | Lewis Acids - chemistry | Fullerenes - isolation & purification | Organosilicon Compounds - chemistry | Oxidation-Reduction | Chromatography, High Pressure Liquid | Fullerenes - chemistry | Photochemical Processes | Separation | Purification | Metallofullerenes | Liquid chromatography | High-performance liquid chromatography | Chromatography | Electrode potentials | Reduction (metal working) | Efficiency | Fullerenes | Electrochemistry | Oxidation | Methods | High performance liquid chromatography
Journal Article
Organic Letters, ISSN 1523-7060, 05/2011, Volume 13, Issue 9, pp. 2480 - 2483
A simple and realistic model for the shortest sidewall segments of chiral single-walled carbon nanotubes (SWNTs) has been designed, and one of the chiral...
HYDROCARBONS | MACROCYCLES | GROWTH | CHEMISTRY, ORGANIC | BELTS | PORPHYRIN | SHAPE-PERSISTENT | TETRADEHYDRODIANTHRACENE
HYDROCARBONS | MACROCYCLES | GROWTH | CHEMISTRY, ORGANIC | BELTS | PORPHYRIN | SHAPE-PERSISTENT | TETRADEHYDRODIANTHRACENE
Journal Article
ChemPhysChem, ISSN 1439-4235, 01/2018, Volume 19, Issue 2, pp. 237 - 242
We investigated the energetics and electronic structure of B3N3‐doped graphene employing density functional theory calculations with the generalized gradient...
density functional theory calculations | band-gap engineering | BNC hererosheet | graphene | electronic structure | ELECTRIC-FIELD | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | STATE | SHEET | STACKED GRAPHENE | BILAYER GRAPHENE | LAYERS | BORON-NITRIDE | MAGNETIC-PROPERTIES | EDGE | Density functionals | Graphene | Specific gravity | Graphite
density functional theory calculations | band-gap engineering | BNC hererosheet | graphene | electronic structure | ELECTRIC-FIELD | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | STATE | SHEET | STACKED GRAPHENE | BILAYER GRAPHENE | LAYERS | BORON-NITRIDE | MAGNETIC-PROPERTIES | EDGE | Density functionals | Graphene | Specific gravity | Graphite
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 08/2012, Volume 10, Issue 30, pp. 5979 - 5984
We studied the UV-vis absorption and fluorescence in solution/solid states of [n]cycloparaphenylene ([n] CPP: n = 9, 12, 14, 15, and 16), and conducted...
DENSITY | ELECTRONIC-PROPERTIES | CONJUGATED SYSTEMS | MACROCYCLES | AB-INITIO | CHEMISTRY, ORGANIC | SELECTIVE SYNTHESIS | CARBON NANOTUBES | TETRADEHYDRODIANTHRACENE | NANORINGS | BOTTOM-UP SYNTHESIS
DENSITY | ELECTRONIC-PROPERTIES | CONJUGATED SYSTEMS | MACROCYCLES | AB-INITIO | CHEMISTRY, ORGANIC | SELECTIVE SYNTHESIS | CARBON NANOTUBES | TETRADEHYDRODIANTHRACENE | NANORINGS | BOTTOM-UP SYNTHESIS
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 31, pp. 3823 - 3826
1,6-Bis(hydroxymethyl)diamantane spontaneously aligns inside double-walled carbon nanotubes. The encapsulated molecules form a one-dimensional network within...
NANORIBBONS | NANODIAMONDS | CHAINS | ADAMANTANE | NANOWIRES | CHEMISTRY, MULTIDISCIPLINARY | MOLECULES | WATER | Encapsulation | Carbon nanotubes | Chemical bonds | Hydrogen bonding | Carbon | Nanotubes
NANORIBBONS | NANODIAMONDS | CHAINS | ADAMANTANE | NANOWIRES | CHEMISTRY, MULTIDISCIPLINARY | MOLECULES | WATER | Encapsulation | Carbon nanotubes | Chemical bonds | Hydrogen bonding | Carbon | Nanotubes
Journal Article
Chemistry Letters, ISSN 0366-7022, 01/2018, Volume 47, Issue 8, p. 1022
We developed the synthesis of one-dimensional polythiophenes inside single-wall carbon nanotubes (SWCNTs). Direct vapor-phase reaction with dibromobithiophenes...
Chemical industry | Bromine | Polythiophene | Tethering | Raman spectroscopy | Chemical synthesis | Single wall carbon nanotubes
Chemical industry | Bromine | Polythiophene | Tethering | Raman spectroscopy | Chemical synthesis | Single wall carbon nanotubes
Journal Article
Journal of Biomaterials Science, Polymer Edition, ISSN 0920-5063, 08/2017, Volume 28, Issue 10-12, pp. 1036 - 1050
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2015, Volume 54, Issue 37, pp. 10802 - 10806
A simple method for the synthesis of linear‐chain diamond‐like nanomaterials, so‐called diamantane polymers, is described. This synthetic approach is primarily...
template synthesis | polymers | carbon nanotubes | radicals | nanodiamonds | GRAPHENE NANORIBBONS | DIAMONDOIDS | RING-OPENING POLYMERIZATION | FABRICATION | METAL NANOWIRES | CHEMISTRY, MULTIDISCIPLINARY | HIGH-YIELD SYNTHESIS | Electron microscopy | Polymers | Nanotubes | Nanomaterials | Carbon | Nanotechnology | Synthesis | Precursors | Diamonds | Carbon nanotubes | Strategy | Holes
template synthesis | polymers | carbon nanotubes | radicals | nanodiamonds | GRAPHENE NANORIBBONS | DIAMONDOIDS | RING-OPENING POLYMERIZATION | FABRICATION | METAL NANOWIRES | CHEMISTRY, MULTIDISCIPLINARY | HIGH-YIELD SYNTHESIS | Electron microscopy | Polymers | Nanotubes | Nanomaterials | Carbon | Nanotechnology | Synthesis | Precursors | Diamonds | Carbon nanotubes | Strategy | Holes
Journal Article