Unravelling the Superiority of Nonbenzenoid Acepleiadylene as a Building Block for Organic Semiconducting Materials** DOI
Lin Fu, Pengcai Liu, Xue Rui

et al.

Angewandte Chemie, Journal Year: 2023, Volume and Issue: 135(36)

Published: July 7, 2023

Abstract Acepleiadylene (APD), a nonbenzenoid isomer of pyrene, exhibits unique charge‐separated character with large molecular dipole and small optical gap. However, APD has never been explored in optoelectronic materials to take advantage these appealing properties. Here, we employ as building block organic semiconducting for the first time, unravel superiority electronic applications. We have synthesized an derivative (APD‐IID) terminal donor moieties isoindigo (IID) acceptor core. Theoretical experimental investigations reveal that APD‐IID obvious structure enhanced intermolecular interactions compared its pyrene‐based isomers. As result, displays significantly higher hole mobilities than those counterparts. These results imply advantages employing great potential polycyclic arenes

Language: Английский

π‐Extended Diaza[7]helicenes with Dual Negatively Curved Heptagons: Extensive Synthesis and Spontaneous Resolution into Strippable Homochiral Lamellae with Helical Symmetry DOI
Fuwei Gan,

Guoli Zhang,

Juncong Liang

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(11)

Published: Jan. 17, 2024

Abstract We report a unique category of π‐extended diaza[7]helicenes with double negative curvatures. This is achieved by two‐fold regioselective heptagonal cyclization the oligoarylene‐carbazole precursors through either intramolecular C−H arylation or Scholl reaction. The fusion two rings in helical skeleton dramatically increases strain and forces terminal carbazole moieties to stack compressed fashion. presence deformable negatively curved endows resulting dynamic chiral skeletons, aggregation‐induced emission feature relatively low racemization barrier ca. 25.6 kcal mol −1 . Further π‐extension on subsequently leads more sophisticated C 2 ‐symmetric homochiral triple helicene. Notably, these show structure‐dependent stacking upon crystallization, switching from heterochiral packing intra‐layer stacking. Interestingly, helicene molecules spontaneously resolve into lamellar structure 3 1 helix symmetry. Upon ultrasonication nonsolvent, crystals can be readily exfoliated large‐area ultrathin nanosheets height 4.4 nm corresponding layers stacked thicker constituted even‐numbered molecular lamellae. Moreover, regular hexagonal thin platelets size larger than 30 μm fabricated flash aggregation.

Language: Английский

Citations

20

Helicoselective Synthesis of Indolohelicenoids through Organocatalytic Central‐to‐Helical Chirality Conversion DOI
Wenlei Xu,

Ru‐Xia Zhang,

Hui Wang

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(9)

Published: Jan. 10, 2024

We report the helicoselective and convergent construction of indolohelicenoids with excellent efficiency stereocontrol. This reaction proceeds through a chiral-phosphoric-acid-catalyzed enantioselective cycloaddition eliminative aromatization sequence, which can be finely controlled by adjusting temperature. Mechanistic studies reveal that chiral phosphoric acid cooperatively serves as both bifunctional Brønsted catalyst, enabling one-pot central-to-helical chirality conversion. Additionally, optical properties synthesized were characterized to explore their potential applications in organic photoelectric materials.

Language: Английский

Citations

9

All Carbon Helicenes and π‐Extended Helicene Derivatives DOI

Li‐Jun Peng,

Xinyue Wang,

Zhi‐Ao Li

et al.

Asian Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 12(12)

Published: Nov. 21, 2023

Abstract Atomic precise chiral molecules with all‐hydrocarbon backbones, such as helicenes and related π‐extended derivatives, attract critical interests due to their great application potential in many fields (e. g., optical materials, asymmetric catalysis, molecular machines). Herein, the main development of these past decade was summarizes, including enantioselective synthesis helicenes, helicene extension along perpendicular helical axis, well following both directions, namely helix axis direction.

Language: Английский

Citations

13

Oxepine-Based π-Conjugated Ladder/Step-Ladder Polymers with Excited -State Aromaticity DOI
Nathan Man‐Wai Wu, Molly C. Warndorf, Alfredo Alexander‐Katz

et al.

Macromolecules, Journal Year: 2024, Volume and Issue: 57(3), P. 991 - 1000

Published: Jan. 24, 2024

Ladder polymers with backbones of uninterrupted ring-fused units have attracted academic and industrial attention for decades because their extended π-conjugation intrinsic microporosity possible potential applications in organic optoelectronics membrane gas separations. We report herein the synthesis characterization a new series oxepine-based ladder/step-ladder prepared by acid-promoted intramolecular aromatic electrophilic cyclization reactions on alkyne-containing poly(arylene ether) precursors. In contrast to more common annulations that produce five- six-membered rings, we seven-membered ring can be regioselectively quantitatively generated postpolymerization. Model compounds repeating also been synthesized, X-ray crystallographic analysis reveals nonplanar contorted structure is present polymers. More interestingly, appear display photoinduced planarization 8 π electron oxepine driven excited-state stabilization energy, as indicated large Stokes shift.

Language: Английский

Citations

5

Investigating the diastereoselective synthesis of a macrocycle under Curtin–Hammett control DOI Creative Commons

Angus Yeung,

Martijn A. Zwijnenburg, Georgia R. F. Orton

et al.

Chemical Science, Journal Year: 2024, Volume and Issue: 15(15), P. 5516 - 5524

Published: Jan. 1, 2024

The Curtin–Hammett principle is used to understand the diastereoselective synthesis of a heterochiral over homochiral macrocycle, both which are configurationally stable chiral macrocycles.

Language: Английский

Citations

3

Hexadehydro Diels–Alder/Alkynyliodanation Cascade: A Highly Regioselective Entry to Polycyclic Aromatics DOI Creative Commons

Shunya Morohashi,

Liejin Zhou, Kazuya Kanemoto

et al.

Organic Letters, Journal Year: 2025, Volume and Issue: unknown

Published: April 15, 2025

We report here a cascade process integrating the hexadehydro Diels-Alder (HDDA) reaction with alkynyliodanation, enabling efficient synthesis of highly substituted aryl-λ3-iodanes. Heating mixture tetrayne and an alkynylbenziodoxole induces regioselective insertion tetrayne-derived aryne into alkynyl-iodine(III) bond, yielding 1,4-dialkynyl-2-iodanyl-3-aryl(or alkyl)benzene derivative. The unique regiochemistry facilitates subsequent π-extension, allowing divergent access to polyaromatic frameworks, such as helicenes cyclopenta[cd]pyrenes, underscoring utility carboiodanation in complex aromatic synthesis.

Language: Английский

Citations

0

Enantiomer-enriched π-Extended Helicenes with a Perylene Core from Binaphthol: Axial-to-Helical Chirality Transfer with Stepwise Scholl Reaction Mechanism DOI Creative Commons

Zhi‐Ao Li,

Kelin Zhu, Nai‐Te Yao

et al.

Chemical Science, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Axially chiral substrates were transformed into enantiomer-enriched π-extended helicenes via a chiral-transfer-based Scholl reaction, and enantiomers efficiently separated without labor-intensive high-performance liquid chromatography (HPLC).

Language: Английский

Citations

0

Catalytic asymmetric construction of helicenes via transformation of biaryls DOI

Peiling Fan,

Lun Li,

Deyun Qian

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(16), P. 3186 - 3197

Published: Jan. 1, 2024

This review showcases a systematic overview of the available tools for catalytic asymmetric transformation biaryl substrates toward construction challenging enantioenriched helicenes and conceptual aspects associated with each type transformation. Depending on properties nature process, several methodologies have been developed, including olefin metathesis, hydroarylation alkynes, C-X (X = C, O, N) coupling, C-H functionalization. Pioneering studies an array representative reactions are discussed to underscore potential these synthetic protocols.

Language: Английский

Citations

3

One‐Pot Synthesis of Helical Azaheptalene and Chiroptical Switching of an Isolable Radical Cation** DOI

Yuta Nishimura,

Takashi Harimoto, Takanori Suzuki

et al.

Chemistry - A European Journal, Journal Year: 2023, Volume and Issue: 29(48)

Published: June 7, 2023

A nitrogen-centered heptalene, azaheptalene, was designed as a representative of new class redox-responsive molecules with large steric strain that originates from the adjacent seven-membered rings. The pentabenzo derivative azaheptalene efficiently synthesized by palladium-catalyzed one-pot reaction commercially available reagents. Bromination led to mono- and dibrominated derivatives, latter which is interconvertible isolable radical cation species exhibiting near-infrared absorption. Since skeleton shows configurationally stable helicity torsion angle, enantiomers could be successfully separated. Thus, optically pure azaheptalenes P- or M-helicity showed strong chiroptical properties (|gabs |≥0.01), changed an electric potential.

Language: Английский

Citations

7

Lighting up nonbenzenoid acepleiadylene with ultra-narrowband emission through aromaticity modulation DOI
Pengcai Liu, Xiaoyu Tang,

Cheng‐Zhuo Du

et al.

Science China Chemistry, Journal Year: 2023, Volume and Issue: 66(12), P. 3506 - 3510

Published: Nov. 21, 2023

Language: Английский

Citations

7