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1.
Small Methods ; : e2400533, 2024 Jun 14.
Article in English | MEDLINE | ID: mdl-38874104

ABSTRACT

The two-dimensional (2-D) Janus and amphiphilic molybdenum disulfide (MoS2) nanosheet with opposite optical activities on each side (amphichiral) is synthesized by modifying sandwich-like bulk MoS2 with tannic acid and cholesterol through biphasic emulsion method. This new type of amphichiral Janus MoS2 nanosheet consists of a hydrophilic and positive optical activity tannic acid side as well as a hydrophobic and negative optical activity cholesterol side thereby characterized by circular dichroism. Surface-directed orientational differentiation assemblies are performed for the as-synthesized 2D material and are characterized by contact angle, infrared spectroscopy, X-ray photoelectron, and circular dichroism spectroscopies. The amphiphilic nature of the materials is demonstrated by the pre-organization of the nanosheets on either hydrophobic or hydrophilic surfaces, providing unprecedented properties of circular dichroism signal enhancement and wettability. Selective detachment of the surface organic groups (cholesterol and tannic acid fragments) is realized by matrix-assisted laser desorption/ionisation - time-of-flight (MALDI-TOF) mass spectrometry, and the dual substrate release in tissue is detected by ex vivo mass spectrometry imaging.

2.
Nat Chem ; 13(3): 255-259, 2021 03.
Article in English | MEDLINE | ID: mdl-33495606

ABSTRACT

The structure-selective precise synthesis of carbon nanotubes (CNTs) has been long sought in materials science. The aromatic molecules corresponding to segment structures of CNTs, that is, carbon nanobelts (CNBs), are of interest as templates for CNT growth. Among the three types of CNB (armchair, chiral and zigzag CNBs), zigzag CNBs have been considered the most difficult type to synthesize. Here we report the synthesis, isolation and structural characterization of a zigzag CNB. The synthesis involves an iterative Diels-Alder reaction sequence followed by reductive aromatization of oxygen-bridged moieties. As predicted by theoretical calculations, this CNB was isolated as a stable compound. The structure of the zigzag CNB was fully characterized by X-ray crystallography and its wide energy gap with blue fluorescence properties was revealed by photophysical measurements. With synthetic strategies towards all three types of CNB in hand, the road to the precise synthesis of CNTs can now proceed to the next stage.

3.
Chemistry ; 26(65): 14791-14801, 2020 Nov 20.
Article in English | MEDLINE | ID: mdl-32572996

ABSTRACT

The development of carbon nanobelts and related belt-shaped polycyclic aromatic hydrocarbons has gained momentum in recent years. This Minireview focuses on the synthetic strategies used in constructing these aesthetically appealing molecular nanocarbons. Examples of carbon nanobelts and related belt-shaped polycyclic aromatic hydrocarbons reported in recent years as well as some representative synthetic attempts in earlier times are discussed.

4.
Angew Chem Int Ed Engl ; 56(31): 9003-9007, 2017 07 24.
Article in English | MEDLINE | ID: mdl-28471075

ABSTRACT

Herein we report synthesis, structure and properties of a new type of twisted nanographene, which contains an [8]circulene moiety in a polycyclic framework of 96 sp2 carbon atoms. The key steps in this synthesis are the Diels-Alder reaction of a macrocyclic diyne and the subsequent Scholl reaction forming the [8]circulene moiety. Two incompletely cyclized products were isolated from the Scholl reaction, providing insight into the cyclization of the strained octagon. This nanographene is twisted along two directions with end-to-end twists of 142.4° and 140.2° as revealed by X-ray crystallography, and is flexible at room temperature as found from the computational and experimental studies.

5.
J Am Chem Soc ; 137(11): 3910-4, 2015 Mar 25.
Article in English | MEDLINE | ID: mdl-25741577

ABSTRACT

Soluble derivatives of C70H26 (1a,b) and C70H30 (2a,b), two new saddle-shaped polycyclic arenes containing two heptagons, were successfully synthesized from saddle-shaped diketones (3a,b), whose carbonyl groups are the key in the reactions to extend the polycyclic π-framework. As found from the crystal structures, the polycyclic backbone of 1b has a deep saddle shape, while that of 2b is even more distorted because of the existence of two [4]-helicene moieties. On the basis of crystal structures, local aromaticity and nonplanarity of individual rings in the saddle-shaped π-backbone were analyzed, and were found to follow Clar's rule in general. It was found that 1b and 3b behaved as p-type semiconductors in solution-processed thin film transistors while the amorphous films of 2b appeared insulating.

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