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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Azulene‐Based Molecules, Polymers, and Frameworks for Optoelectronic and Energy Applications
Jiaqian Huang, Senhe Huang, Yazhen Zhao, et al.
Small Methods (2020) Vol. 4, Iss. 10
Closed Access | Times Cited: 59

Showing 26-50 of 59 citing articles:

Azulene, Reactivity, and Scientific Interest Inversely Proportional to Ring Size; Part 1: The Five-Membered Ring
Alexandru C. Razus
Symmetry (2023) Vol. 15, Iss. 2, pp. 310-310
Open Access | Times Cited: 5
Lighting up nonbenzenoid acepleiadylene with ultra-narrowband emission through aromaticity modulation
Pengcai Liu, Xiaoyu Tang, Cheng‐Zhuo Du, et al.
Science China Chemistry (2023) Vol. 66, Iss. 12, pp. 3506-3510
Closed Access | Times Cited: 5
Highly Selective On-Surface Ring-Opening of Aromatic Azulene Moiety
Lulu Wang, Xinnan Peng, Jie Su, et al.
Journal of the American Chemical Society (2023) Vol. 146, Iss. 2, pp. 1563-1571
Closed Access | Times Cited: 5
Tuning the redox profile of the 6,6′-biazulenic platform through functionalization along its molecular axis
Shaun Kelsey, Георгий Д. Грязнов, Andrew D. Spaeth, et al.
Chemical Communications (2024) Vol. 60, Iss. 39, pp. 5213-5216
Open Access | Times Cited: 1
Synthesis and properties of 2,6-azulene-based conjugated polymers and their applications in dispersing single-walled carbon nanotubes
Guillaume Chamelot, Maël Idir, Mario Leclerc, et al.
Polymer Chemistry (2023) Vol. 14, Iss. 11, pp. 1206-1212
Closed Access | Times Cited: 4
Unravelling the Superiority of Nonbenzenoid Acepleiadylene as a Building Block for Organic Semiconducting Materials**
Lin Fu, Pengcai Liu, Xue Rui, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 36
Closed Access | Times Cited: 4
Azulene-Fused Linearly π-Extended Polycyclic Aromatic Compounds: Synthesis, Photophysical Properties, and OFETs Applications
Masahito Murai, Shinji Iba, Shino Hamao, et al.
Bulletin of the Chemical Society of Japan (2023) Vol. 96, Iss. 9, pp. 1077-1081
Open Access | Times Cited: 4
Redox‐Active Azulene‐based 2D Conjugated Covalent Organic Framework for Organic Memristors
Zhao Zhizheng, Mohamed E. El‐Khouly, Qiang Che, et al.
Angewandte Chemie (2022) Vol. 135, Iss. 7
Closed Access | Times Cited: 7
Tuning the edge states in X-type carbon based molecules for applications in nonlinear optics
Cuicui Yang, Xue-Lian Zheng, Wei Quan Tian, et al.
Physical Chemistry Chemical Physics (2021) Vol. 24, Iss. 13, pp. 7713-7722
Closed Access | Times Cited: 10
Chemical syntheses and salient features of azulene-containing homo- and copolymers
Vijayendra S. Shetti
Beilstein Journal of Organic Chemistry (2021) Vol. 17, pp. 2164-2185
Open Access | Times Cited: 10
Second order nonlinear optical properties of poled films containing azobenzenes tailored with azulen-1-yl-pyridine
Ana‐Maria Manea‐Saghin, Adrian Ion, François Kajzar, et al.
Heliyon (2023) Vol. 9, Iss. 6, pp. e17360-e17360
Open Access | Times Cited: 3
Azulene, Reactivity, and Scientific Interest Inversely Proportional to Ring Size; Part 2: The Seven-Membered Ring
Alexandru C. Razus
Symmetry (2023) Vol. 15, Iss. 7, pp. 1391-1391
Open Access | Times Cited: 3
Dancing with Azulene
Alexandru C. Razus
Symmetry (2022) Vol. 14, Iss. 2, pp. 297-297
Open Access | Times Cited: 5
Cascade Synthesis of Benzotriazulene with Three Embedded Azulene Units and Large Stokes Shifts
Yimin Liang, Shangshang Wang, Min Tang, et al.
Angewandte Chemie (2023) Vol. 135, Iss. 25
Closed Access | Times Cited: 2
Artificial Design of Organic Emitters via a Genetic Algorithm Enhanced by a Deep Neural Network
AkshatKumar Nigam, Robert Pollice, Pascal Friederich, et al.
(2023)
Open Access | Times Cited: 2
Liquid-Phase Exfoliation of Graphite in a Low-Boiling-Point Solvent Using 2,6-Azulene-Based Conjugated Copolymers as Stabilizers
Guillaume Chamelot, Maël Idir, William R. Leonard, et al.
ACS Applied Polymer Materials (2023) Vol. 6, Iss. 1, pp. 170-179
Closed Access | Times Cited: 2
Solvent-free C–H alkynylation of azulenes
Agata Jarszak-Tyl, Bartłomiej Pigulski, Sławomir Szafert
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 20, pp. 5674-5680
Closed Access | Times Cited: 5
Poly(2-aminoazulene) Filler–Improved PEO-Based Electrolyte for Highly Stable Solid-State Li-Metal Batteries
Jia Wen, Zhenying Chen, Sheng Han, et al.
Journal of The Electrochemical Society (2021) Vol. 168, Iss. 9, pp. 090545-090545
Closed Access | Times Cited: 5
Tailoring Band Gaps in Thienyltriazine based Conjugated Porous Polymers through Comonomer Variation
Neha Rani Kumar, Abhijeet R. Agrawal, Himadri S. Karmakar, et al.
ChemistrySelect (2024) Vol. 9, Iss. 7
Closed Access
From Plant Oils to High‐Performance Supercapacitor Electrode: Poly(guaiazulene) via Photopolymerization
Sena Ermis, Sinem Altınışık, Fahri Çatoğlu, et al.
Advanced Electronic Materials (2024)
Open Access
Hydrophilization of hydrophobic azulene derivative by substitution with polyallylamine without drastically changing its optical properties
Yo Kinoshita, Kiyotaka Maruoka, Y. Takahashi, et al.
MRS Communications (2024)
Closed Access
Properties Assessment by Quantum Mechanical Calculations for Azulenes Substituted with Thiophen– or Furan–Vinyl–Pyridine
Oana Ciocîrlan, Eleonora‐Mihaela Ungureanu, Alina-Alexandra Vasile, et al.
Symmetry (2022) Vol. 14, Iss. 2, pp. 354-354
Open Access | Times Cited: 3
Merging of Azulene and Perylene Diimide for Optical pH Sensors
Ping Zhou, Ulrich Aschauer, Silvio Decurtins, et al.
(2023)
Open Access | Times Cited: 1
Functionalized Poly(azulenes) and Their Electrochromic Properties
Zhuang Mao Png, Georgina E. K. K. Seah, Ming Hui Chua, et al.
ChemistrySelect (2023) Vol. 8, Iss. 45
Closed Access | Times Cited: 1
Utilization of the through-space effect to design donor–acceptor systems of pyrrole, indole, isoindole, azulene and aniline
Puthannur K. Anjalikrishna, Cherumuttathu H. Suresh
Physical Chemistry Chemical Physics (2023) Vol. 26, Iss. 2, pp. 1340-1351
Closed Access | Times Cited: 1

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