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For: Rosenberg M, Santella M, Bogh SA, Muñoz AV, Andersen HOB, Hammerich O, Bora I, Lincke K, Laursen BW. Extended Triangulenium Ions: Syntheses and Characterization of Benzo-Bridged Dioxa- and Diazatriangulenium Dyes. J Org Chem 2019;84:2556-67. [PMID: 30694674 DOI: 10.1021/acs.joc.8b02978] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Poronik YM, Ambicki F, Tseng SM, Chou PT, Deperasińska I, Gryko DT. How an Eight-Membered Ring Alters the Rhodamine Chromophore. J Org Chem 2020;85:5973-80. [PMID: 32252525 DOI: 10.1021/acs.joc.0c00414] [Reference Citation Analysis]
2 Jensen JD, Bisballe N, Kacenauskaite L, Thomsen MS, Chen J, Hammerich O, Laursen BW. Utilizing Selective Chlorination to Synthesize New Triangulenium Dyes. J Org Chem 2021;86:17002-10. [PMID: 34791879 DOI: 10.1021/acs.joc.1c02148] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Holt CJ, Wentworth KJ, Johnson RP. A Short and Efficient Synthesis of the [3]Triangulene Ring System. Angew Chem Int Ed 2019;58:15793-6. [DOI: 10.1002/anie.201907226] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
4 Hammerich O, Nielsen MB. Extended tetrathiafulvalenes with polycyclic aromatic cores. J Mater Chem C 2019;7:2809-22. [DOI: 10.1039/c9tc00120d] [Cited by in Crossref: 18] [Cited by in F6Publishing: 1] [Article Influence: 6.0] [Reference Citation Analysis]
5 Borissov A, Maurya YK, Moshniaha L, Wong WS, Żyła-Karwowska M, Stępień M. Recent Advances in Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds. Chem Rev 2021. [PMID: 34850633 DOI: 10.1021/acs.chemrev.1c00449] [Reference Citation Analysis]
6 Lewis BW, Bisballe N, Santella M, Summers PA, Vannier JB, Kuimova MK, Laursen BW, Vilar R. Assessing The Key Photophysical Properties of Triangulenium Dyes for DNA Binding by Alteration of the Fluorescent Core. Chemistry 2021;27:2523-36. [PMID: 33105523 DOI: 10.1002/chem.202003875] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Bisballe N, Laursen BW. What is Best Strategy for Water Soluble Fluorescence Dyes?-A Case Study Using Long Fluorescence Lifetime DAOTA Dyes*. Chemistry 2020;26:15969-76. [PMID: 32639046 DOI: 10.1002/chem.202002457] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Bartoš D, Rewers M, Wang L, Sørensen TJ. Incorporating fluorescent nanomaterials in organically modified sol–gel materials – creating single composite optical pH sensors. Sens Diagn 2022;1:185-92. [DOI: 10.1039/d1sd00002k] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Hutskalova V, Prescimone A, Sparr C. Synthesis of Helical and Planar Extended‐Phenanthridinium Salts. Helvetica Chimica Acta 2021;104. [DOI: 10.1002/hlca.202100182] [Reference Citation Analysis]
10 Laursen BW, Bogh SA, Sørensen TJ. Long fluorescence lifetime triangulenium dyes in imaging and fluorescence polarization assay. Methods Enzymol 2020;640:249-65. [PMID: 32560801 DOI: 10.1016/bs.mie.2020.04.031] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
11 Barsuk I, Lainé PP, Maurel F, Brémond É. Triangulenium dyes: the comprehensive photo-absorption and emission story of a versatile family of chromophores. Phys Chem Chem Phys 2020;22:20673-84. [PMID: 32895673 DOI: 10.1039/d0cp02990d] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
12 Marinova M, Pascal S, Guénée L, Besnard C, Shivachev B, Kostova K, Villani C, Franzini R, Dimitrov V, Lacour J. Synthesis, Resolution, Configurational Stability, and Properties of Cationic Functionalized [5]Helicenes. J Org Chem 2020;85:11908-23. [PMID: 32907321 DOI: 10.1021/acs.joc.0c01716] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
13 Santella M, Della Pia E, Sørensen JK, Laursen BW. Synthesis and properties of sulfur-functionalized triarylmethylium, acridinium and triangulenium dyes. Beilstein J Org Chem 2019;15:2133-41. [PMID: 31579076 DOI: 10.3762/bjoc.15.210] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]