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:

Fluorinated antimony(v) derivatives: strong Lewis acidic properties and application to the complexation of formaldehyde in aqueous solutions
Daniel Tofan, François P. Gabbaı̈
Chemical Science (2016) Vol. 7, Iss. 11, pp. 6768-6778
Open Access | Times Cited: 75

Showing 26-50 of 75 citing articles:

Pnictogen bonding at the service of gold catalysis: the case of a phosphinostiborane gold complex
Benyu Zhou, Shantabh Bedajna, François P. Gabbaı̈
Chemical Communications (2023) Vol. 60, Iss. 2, pp. 192-195
Closed Access | Times Cited: 7

Hydrogen activation using a novel tribenzyltin Lewis acid
Robert T. Cooper, Joshua S. Sapsford, Roland C. Turnell‐Ritson, et al.
Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences (2017) Vol. 375, Iss. 2101, pp. 20170008-20170008
Open Access | Times Cited: 23

Nitrenium Salts in Lewis Acid Catalysis
Meera Mehta, José M. Goicoechea
Angewandte Chemie (2019) Vol. 132, Iss. 7, pp. 2737-2741
Open Access | Times Cited: 21

A Stiboranyl Platinum Triflate Complex as an Electrophilic Catalyst
Di You, Jesse E. Smith, Srobona Sen, et al.
Organometallics (2020) Vol. 39, Iss. 23, pp. 4169-4173
Closed Access | Times Cited: 19

Oxidation-dependent Lewis acidity in chalcogen adducts of Sb/P frustrated Lewis pairs
Jonas Krieft, Beate Neumann, Hans‐Georg Stammler, et al.
Dalton Transactions (2024) Vol. 53, Iss. 28, pp. 11762-11768
Open Access | Times Cited: 2

Digging the Sigma‐Hole of Organoantimony Lewis Acids by Oxidation
Mengxi Yang, Daniel Tofan, Chang-Hung Chen, et al.
Angewandte Chemie (2018) Vol. 130, Iss. 42, pp. 14064-14068
Closed Access | Times Cited: 20

Crystallographic evidence for a continuum and reversal of roles in primary–secondary interactions in antimony Lewis acids: applications in carbonyl activation
Deepti Sharma, Annabel Benny, Radhika Gupta, et al.
Chemical Communications (2022) Vol. 58, Iss. 78, pp. 11009-11012
Closed Access | Times Cited: 10

The Lewis superacidic aluminium cation: [(NHC)Al(C6F5)2]+
Shaoying Ju, Chi Zhang, Beili Tang, et al.
Chemical Communications (2023) Vol. 60, Iss. 6, pp. 698-701
Closed Access | Times Cited: 6

Binuclear Triphenylantimony(V) Catecholate Based on Redox-Active Bis-o-Benzoquinone, a Bis-Catechol-Aldimine Derivative
M. V. Arsen’ev, L. S. Okhlopkova, A. I. Poddel’skii, et al.
Russian Journal of Coordination Chemistry (2018) Vol. 44, Iss. 2, pp. 162-168
Closed Access | Times Cited: 17

Bis(perchlorocatecholato)silane and heteroleptic bidonors: hidden frustrated Lewis pairs resulting from ring strain
Deborah Hartmann, Sven Braner, Lutz Greb
Chemical Communications (2021) Vol. 57, Iss. 69, pp. 8572-8575
Closed Access | Times Cited: 14

Hydroalumination of 1,8-Diethynylanthracenes–Al-based Bis-Lewis-Acids and their Isomerization and Complexation Behavior
Niklas Aders, Pia C. Trapp, Jan‐Hendrik Lamm, et al.
Organometallics (2022) Vol. 41, Iss. 23, pp. 3600-3611
Closed Access | Times Cited: 9

Interaction of formaldehyde with a water-tolerant frustrated Lewis pair
Ghazi Ghattas, Claudia Bizzarri, Markus Hölscher, et al.
Chemical Communications (2017) Vol. 53, Iss. 22, pp. 3205-3208
Closed Access | Times Cited: 16

Establishing the Role of Triflate Anions in H2 Activation by a Cationic Triorganotin(IV) Lewis Acid
Joshua S. Sapsford, Dániel Csókás, Daniel J. Scott, et al.
ACS Catalysis (2020) Vol. 10, Iss. 14, pp. 7573-7583
Open Access | Times Cited: 13

Triphenylantimony(V) catecholato complexes with 4-(2,6-dimethylphenyliminomethyl)pyridine. Structure, redox properties: The influence of pyridine ligand
L. S. Okhlopkova, Andrey I. Poddel’sky, Ivan V. Smolyaninov, et al.
Journal of Organometallic Chemistry (2019) Vol. 897, pp. 32-41
Closed Access | Times Cited: 13

Applications of Antimony in Catalysis
Liji Wu, Choon‐Hong Tan, Xinyi Ye
ACS Organic & Inorganic Au (2024) Vol. 5, Iss. 1, pp. 13-25
Open Access | Times Cited: 1

Steric Selection of Anion Binding Sites by Organoantimony(V) Pnictogen Bond Donors: An Experimental and Computational Study
Brendan L. Murphy, Logan T. Maltz, François P. Gabbaı̈
Inorganic Chemistry (2024)
Open Access | Times Cited: 1

Attempted synthesis of ortho -phenylene phosphino-tritylium cations
Kantapat Chansaenpak, Mengxi Yang, François P. Gabbaı̈
Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences (2017) Vol. 375, Iss. 2101, pp. 20170007-20170007
Open Access | Times Cited: 10

New catecholate complexes of triphenylantimony(V) based on 6-iminomethyl-3,5-di-tert-butylpyrocatechols N-functionalized by the aniline or phenol group
Andrey I. Poddel’sky, M. V. Arsen’ev, L. S. Okhlopkova, et al.
Russian Journal of Coordination Chemistry (2017) Vol. 43, Iss. 12, pp. 843-851
Closed Access | Times Cited: 10

Interaction between Spirosilanes and Lewis Bases: from Coordination to Frustration
Fabrizio Medici, Julien Maury, Gilles Lemière, et al.
Chemistry - A European Journal (2019) Vol. 25, Iss. 40, pp. 9438-9442
Open Access | Times Cited: 10

Triphenylantimony(V) Catecholates Based on o-Quinones, Derivatives of Benzo[b][1,4]-Dioxines and Benzo[b][1,4]-Dioxepines
A. I. Poddel’skii, L. S. Okhlopkova, Irina N. Meshcheryakova, et al.
Russian Journal of Coordination Chemistry (2019) Vol. 45, Iss. 2, pp. 133-141
Closed Access | Times Cited: 10

Arylantimony Derivatives of Three-Coordinated Carbon
В.В. Шарутин, О.К. Шарутина, А.Н. Ефремов
Russian Journal of Inorganic Chemistry (2020) Vol. 65, Iss. 1, pp. 45-51
Closed Access | Times Cited: 10

Triphenylantimony(V) Catecholates of the Type (3-RS-4,6-DBCat)SbPh3-Catechol Thioether Derivatives: Structure, Electrochemical Properties, and Antiradical Activity
Ivan V. Smolyaninov, Georgy K. Fukin, Н. Т. Берберова, et al.
Molecules (2021) Vol. 26, Iss. 8, pp. 2171-2171
Open Access | Times Cited: 8

Synthesis, Structure, Reactivity, and Intramolecular Donor–Acceptor Interactions in a Phosphinoferrocene Stibine and Its Corresponding Phosphine Chalcogenides and Stiboranes
Jiří Schulz, Jakub Antala, David Rezazgui, et al.
Inorganic Chemistry (2023) Vol. 62, Iss. 34, pp. 14028-14043
Open Access | Times Cited: 3

Increasing Lewis acidity in perchlorophenyl derivatives of antimony
M.A. Garcia-Monforte, Miguel Baya, Daniel Joven‐Sancho, et al.
Journal of Organometallic Chemistry (2019) Vol. 897, pp. 185-191
Closed Access | Times Cited: 8

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