Selectivity control towards CO versus H₂ for photo-driven CO₂ reduction with a novel Co(II) catalyst

• Lisa-Lou Gracia,
• Philip Henkel,
• Olaf Fuhr and
• Claudia Bizzarri

Beilstein J. Org. Chem. 2023, 19, 1766–1775, doi:10.3762/bjoc.19.129

• inside for at least 10 minutes. TEA or TEOA was distilled twice before use. Experiments were performed in a photoreactor from Luzchem (model: LZC-ICH2) equipped with two lamps at 420 nm (fluorescent lamps of 8 W each) and four mini-stirrers. On each stirrer, two samples were irradiated at the same time

Quinoxaline derivatives as attractive electron-transporting materials

• Zeeshan Abid,
• Liaqat Ali,
• Sughra Gulzar,
• Faiza Wahad,
• Raja Shahid Ashraf and
• Christian B. Nielsen

Beilstein J. Org. Chem. 2023, 19, 1694–1712, doi:10.3762/bjoc.19.124

• -phenylindoloquinoxaline (PhIQ) derivatives, shown in Figure 6 as Qx50 series, by chemically modifying the PhIQ groups. In particular, substituents at the 2- and 3-positions of PhIQs were introduced, allowing regulation of the reduction–oxidation potentials of the compounds. The PhIQs exhibited fluorescent solvatochromism

A deep-red fluorophore based on naphthothiadiazole as emitter with hybridized local and charge transfer and ambipolar transporting properties for electroluminescent devices

• Suangsiri Arunlimsawat,
• Patteera Funchien,
• Pongsakorn Chasing,
• Atthapon Saenubol,
• Taweesak Sudyoadsuk and
• Vinich Promarak

Beilstein J. Org. Chem. 2023, 19, 1664–1676, doi:10.3762/bjoc.19.122

• = 20%, PLQY in a thin film = 35%, and charge recombination: ηrec = 100%) to be 47%. This EUE was higher than the 25% theoretical upper limit of spin statistics for typical fluorescent emitters, indicating that the triplet excitons have been utilized via an HLCT mechanism to contribute to the EL in this

Tying a knot between crown ethers and porphyrins

• Maksym Matviyishyn and
• Bartosz Szyszko

Beilstein J. Org. Chem. 2023, 19, 1630–1650, doi:10.3762/bjoc.19.120

• the dipyrrin part of the macrocycle (Figure 4). The introduction of the BF2 moiety into the free-base macrocycles consequently altered the fluorescent properties of the macrocyclic systems. The appended benzo-18-crown-6 in compounds 3a–c was selective for K+, and the macrocycle fluorescence was

• ether systems, where the catechol unit of the crown ether was fused to two β-pyrrolic positions of the porphyrin periphery. The systems presented intriguing intramolecular electron-transfer properties. Additionally, they were investigated as fluorescent sensors for various organic and metal cations [51

Synthesis of ether lipids: natural compounds and analogues

• Marco Antônio G. B. Gomes,
• Alicia Bauduin,
• Chloé Le Roux,
• Romain Fouinneteau,
• Wilfried Berthe,
• Mathieu Berchel,
• Hélène Couthon and
• Paul-Alain Jaffrès

Beilstein J. Org. Chem. 2023, 19, 1299–1369, doi:10.3762/bjoc.19.96

Organic thermally activated delayed fluorescence material with strained benzoguanidine donor

• Alexander C. Brannan,
• Elvie F. P. Beaumont,
• Nguyen Le Phuoc,
• George F. S. Whitehead,
• Mikko Linnolahti and
• Alexander S. Romanov

Beilstein J. Org. Chem. 2023, 19, 1289–1298, doi:10.3762/bjoc.19.95

• matrices regardless of numerous efforts and cooling the films down to 16 K and applying long time delays. Conclusion We have synthesized and characterized a donor–acceptor-type thermally activated delayed fluorescent emitter 4BGIPN with four terminal benzoguanidine donor moieties surrounding the

Unravelling a trichloroacetic acid-catalyzed cascade access to benzo[f]chromeno[2,3-h]quinoxalinoporphyrins

• Chandra Sekhar Tekuri,
• Pargat Singh and
• Mahendra Nath

Beilstein J. Org. Chem. 2023, 19, 1216–1224, doi:10.3762/bjoc.19.89

• microbial strains [16][17]. Thorough literature search revealed that the fused heterocycles such as benzo[a]pyrano[2,3-c]phenazines and benzo[a]chromeno[2,3-c]phenazines have been prepared as fluorescent materials [18][19]. On the other hand, xanthenes exhibited a number of biological and pharmaceutical

New one-pot synthesis of 4-arylpyrazolo[3,4-b]pyridin-6-ones based on 5-aminopyrazoles and azlactones

• Vladislav Yu. Shuvalov,
• Ekaterina Yu. Vlasova,
• Tatyana Yu. Zheleznova and
• Alexander S. Fisyuk

Beilstein J. Org. Chem. 2023, 19, 1155–1160, doi:10.3762/bjoc.19.83

• ) under solvent-free conditions, through subsequent elimination of a benzamide molecule in a superbasic medium (t-BuOK/DMSO). The fluorescent properties of the synthesized compounds were studied. 4-Arylpyrazolo[3,4-b]pyridin-6-ones luminesce in the region of 409–440 nm with a quantum yield of 0.09–0.23

• -trimethoxyphenyl- (4e), 2-furyl- (4h) and 2-thienyl- (4i), the product yields are reduced to 55–60% (Scheme 2). All the compounds obtained are colorless crystalline substances. When dissolved, they produce colorless solutions exhibiting distinct fluorescent properties with blue emission when exposed to UV light

A fluorescent probe for detection of Hg²⁺ ions constructed by tetramethyl cucurbit[6]uril and 1,2-bis(4-pyridyl)ethene

• Xiaoqian Chen,
• Naqin Yang,
• Yue Ma,
• Xinan Yang and
• Peihua Ma

Beilstein J. Org. Chem. 2023, 19, 864–872, doi:10.3762/bjoc.19.63

• cucurbit[6]uril (TMeQ[6]) and 1,2-bis(4-pyridyl)ethene (G) were used to construct a supramolecular fluorescent probe G@TMeQ[6]. The host–guest interaction between TMeQ[6] and G was investigated using 1H NMR spectroscopy, single-crystal X-ray diffraction and various experimental techniques. The results show

• that TMeQ[6] and G form an inclusion complex with a host–guest ratio of 1:1 and the equilibrium association constant (Ka) was 2.494 × 104 M−1. The G@TMeQ[6] fluorescent probe can sensitively recognize Hg2+ ions by fluorescence enhancement. The linear range is 0.33 × 10−5–1.65 × 10−5 mol·L−1, R2

• = 0.9926, and the limit of detection is 4.12 × 10−8 mol·L−1. The fluorescent probe can be used to detect the concentration of Hg2+ ions in aqueous solution, and provides a theoretical basis for the development of new fluorescent probes for detecting heavy metal ions. Keywords: 1,2-bis(4-pyridyl)ethane

Strategies in the synthesis of dibenzo[b,f]heteropines

• David I. H. Maier,
• Barend C. B. Bezuidenhoudt and
• Charlene Marais

Beilstein J. Org. Chem. 2023, 19, 700–718, doi:10.3762/bjoc.19.51

• yield proved to be good to excellent and sterically hindered aryl rings were tolerated. This method was applied by Huang et al. [74] to prepare a series of fluorescent compounds in excellent yield. Copper- and nickel-catalysed arylation were reported as alternatives to the Pd-catalysed arylation of 1a

pH-Responsive fluorescent supramolecular nanoparticles based on tetraphenylethylene-labelled chitosan and a six-fold carboxylated tribenzotriquinacene

• Nan Yang,
• Yi-Yan Zhu,
• Wei-Xiu Lin,
• Yi-Long Lu and
• Wen-Rong Xu

Beilstein J. Org. Chem. 2023, 19, 635–645, doi:10.3762/bjoc.19.45

• , PR China 10.3762/bjoc.19.45 Abstract We synthesized a new tetraphenylethylene-modified chitosan bioconjugate, CS-TPE, that shows the aggregation-induced emission effect. It can self-assemble into fluorescent polymeric nanoparticles in an aqueous solution at pH 5.3 either alone or with the water

• based on TBTQ with fluorescent imaging modules that are stable in acidic environments and collapse/swell in alkaline environments. The development of nanoscale drug delivery systems equipped with synchronized fluorescent imaging modules has attracted significant interest in recent years. However

• , conventional fluorescent dyes exhibit aggregation-caused quenching (ACQ) when introduced into nanoparticles at high loads, resulting in poor fluorescence imaging quality. In recent years, tetraphenylethylene (TPE)-based dyes have been frequently used to overcome the ACQ problem due to their unique aggregation

Phenanthridine–pyrene conjugates as fluorescent probes for DNA/RNA and an inactive mutant of dipeptidyl peptidase enzyme

• Josipa Matić,
• Tana Tandarić,
• Marijana Radić Stojković,
• Filip Šupljika,
• Zrinka Karačić,
• Ana Tomašić Paić,
• Lucija Horvat,
• Robert Vianello and
• Lidija-Marija Tumir

Beilstein J. Org. Chem. 2023, 19, 550–565, doi:10.3762/bjoc.19.40

• RNA, single or double-stranded polynucleotides, particular base composition…) and signalize binding by specific spectroscopic response is of great importance [1][2]. Pyrene derivatives are among the earliest known fluorescent probes for biomolecules. These chromophores are often used due to their high

• sensitivity to the polarity of its surroundings. Similar as pyrenes, phenanthridines are also used as fluorescent probes, and their characteristics may be altered by various substituents appended to the aromatic core. The formation of excimers by two or more pyrenes is well known in the literature [4

• -dependent, and the flexibility of the linker can alter that [13]. Further, pyrene-guanidiniocarbonylpyrrole discriminated DNA and RNA by different spectroscopic (induced circular dichroism signal and fluorescent signal) responses [14]. Also, we recently reported a pyrene–quinoline conjugate molecule that

CuAAC-inspired synthesis of 1,2,3-triazole-bridged porphyrin conjugates: an overview

• Dileep Kumar Singh

Beilstein J. Org. Chem. 2023, 19, 349–379, doi:10.3762/bjoc.19.29

• well as optical properties. Moreover, the versatility of coumarin hybrids finds numerous applications including fluorescent brightening agents [16], optical sensors [17], organic light emitting diodes [18][19], light harvesting materials [20] and fluorescent probes in biological imaging [21]. Therefore

• many biological [24] as well as fluorescent properties [25]. Therefore, considering these properties of xanthone, we used a click chemistry protocol to prepare β-triazole-linked porphyrin-xanthone conjugates 23–27 and xanthone-bridged β-triazolobisporphyrin conjugates 28, 29 [26] (Scheme 3). Initially

• 124 in the presence of copper bromide and tris((1-benzyl-4-triazolyl)methyl)amine (TBTA) in DMSO/H2O to give a porphyrin-lantern (PL)-DNA sequence in 45% yield after cleavage and deprotection. These PL-DNA sequences were further used to construct strong and fluorescent G-wires that could be useful for

Sequential hydrozirconation/Pd-catalyzed cross coupling of acyl chlorides towards conjugated (2E,4E)-dienones

• Benedikt Kolb,
• Daniela Silva dos Santos,
• Sanja Krause,
• Anna Zens and
• Sabine Laschat

Beilstein J. Org. Chem. 2023, 19, 176–185, doi:10.3762/bjoc.19.17

• displays pronounced cytotoxicity against two human cancer cell lines [1], epicocconone (2), a fluorescent compound from the fungus Epicoccum nigrum [2], β-ionone (3) from many plant-derived sources [3], epoxysorbicillinol (4) from the saltwater culture of the fungus Trichoderma longibrachiatum separated

Formal total synthesis of macarpine via a Au(I)-catalyzed 6-endo-dig cycloisomerization strategy

• Jiayue Fu,
• Bingbing Li,
• Zefang Zhou,
• Maosheng Cheng,
• Lu Yang and
• Yongxiang Liu

Beilstein J. Org. Chem. 2022, 18, 1589–1595, doi:10.3762/bjoc.18.169

• -inflammatory [4][5][6][7][8], insecticidal, fungicidal, etc [9]. In addition to the above-mentioned activities, macarpine was also used as a DNA probe for flow cytometry and fluorescence microscopy due to its fluorescent properties [10]. Despite some research on the activities of macarpine had been performed

Microelectrode arrays, electrosynthesis, and the optimization of signaling on an inert, stable surface

• Kendra Drayton-White,
• Siyue Liu,
• Yu-Chia Chang,
• Sakashi Uppal and
• Kevin D. Moeller

Beilstein J. Org. Chem. 2022, 18, 1488–1498, doi:10.3762/bjoc.18.156

• peptides were placed on the array along with a fluorescent dye (LRSC, lissamine rhodamine) that was used to make sure the placement chemistry was working. The array used was coated with the borate ester diblock copolymer (Figure 2), and the peptides were attached to this polymer through a PEG-6 linker in

• . 4 cycles. Quantitative fluorescent study on variance of the polymer coating across the microelectrode surface. Purple represents blocks from the top region. Blue represents blocks from the center region. Orange represents blocks from the bottom region. An initial study and the comparison of an R6A

Mechanochemical synthesis of unsymmetrical salens for the preparation of Co–salen complexes and their evaluation as catalysts for the synthesis of α-aryloxy alcohols via asymmetric phenolic kinetic resolution of terminal epoxides

• Shengli Zuo,
• Shuxiang Zheng,
• Jianjun Liu and
• Ang Zuo

Beilstein J. Org. Chem. 2022, 18, 1416–1423, doi:10.3762/bjoc.18.147

• addition, a Lewis basic NEt2 (‒N(CH2CH3)2) group was introduced to the salen scaffold to facilitate purification, enhance catalytic efficiency, and improve the thermal stability, as was shown in the synthesis of fluorescent probes [41][42]. The chelating effect of salen compounds 1 with different metals

Computational model predicts protein binding sites of a luminescent ligand equipped with guanidiniocarbonyl-pyrrole groups

• Neda Rafieiolhosseini,
• Matthias Killa,
• Thorben Neumann,
• Niklas Tötsch,
• Jean-Noël Grad,
• Alexander Höing,
• Thies Dirksmeyer,
• Jochen Niemeyer,
• Christian Ottmann,
• Shirley K. Knauer,
• Michael Giese,
• Jens Voskuhl and
• Daniel Hoffmann

Beilstein J. Org. Chem. 2022, 18, 1322–1331, doi:10.3762/bjoc.18.137

• overcome this issue is to use fluorescence emission as a read-out tool, such as an emission “on” or “off” behavior [15]. Selective and sensitive fluorescent ligands have been proven to be essential tools for the study of biological systems by biosensing and imaging [16]. There is an increasing demand for

Ionic multiresonant thermally activated delayed fluorescence emitters for light emitting electrochemical cells

• Merve Karaman,
• Abhishek Kumar Gupta,
• Subeesh Madayanad Suresh,
• Tomas Matulaitis,
• Lorenzo Mardegan,
• Daniel Tordera,
• Henk J. Bolink,
• Sen Wu,
• Stuart Warriner,
• Ifor D. Samuel and
• Eli Zysman-Colman

Beilstein J. Org. Chem. 2022, 18, 1311–1321, doi:10.3762/bjoc.18.136

• ), Universidad de Valencia, C/Catedrático J. Beltrán 2, 46980 Paterna (Valencia), Spain School of Chemistry, University of Leeds, Woodhouse Lane, Leeds, UK 10.3762/bjoc.18.136 Abstract We designed and synthesized two new ionic thermally activated delayed fluorescent (TADF) emitters that are charged analogues of

• in organic light-emitting diodes (OLEDs), relatively little attention has been devoted to the design of ionic small molecule (SM) [13] organic emitters for LEECs. The majority of the reported SM emitters for LEECs are fluorescent in nature and so the internal quantum efficiency (IQE) of the device is

• limited to 25% [13]. Thermally activated delayed fluorescent (TADF) emitters are one class of purely organic materials that can harvest triplet excitons in electroluminescent (EL) devices through a triplet to singlet reverse intersystem crossing (RISC) upconversion process [14]. Indeed, OLEDs using TADF

Polymer and small molecule mechanochemistry: closer than ever

• José G. Hernández

Beilstein J. Org. Chem. 2022, 18, 1225–1235, doi:10.3762/bjoc.18.128

• fluorescent 9-fluorenone (3) via β-scission (Scheme 1b). To highlight the importance of the polymer network in the transduction of the mechanical stimulus to the mechanophore, the authors demonstrated that ball milling monomeric BMPF-OH at 30 Hz for 3 h only generated traces of 3 (1% after isolation

Synthesis, optical and electrochemical properties of (D–π)₂-type and (D–π)₂Ph-type fluorescent dyes

• Kosuke Takemura,
• Kazuki Ohira,
• Taiki Higashino,
• Keiichi Imato and
• Yousuke Ooyama

Beilstein J. Org. Chem. 2022, 18, 1047–1054, doi:10.3762/bjoc.18.106

• Kosuke Takemura Kazuki Ohira Taiki Higashino Keiichi Imato Yousuke Ooyama Applied Chemistry Program, Graduate School of Advanced Science and Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi-Hiroshima 739-8527, Japan 10.3762/bjoc.18.106 Abstract The (D–π)2-type fluorescent dye OTT-2

• with two (diphenylamino)carbazole-thiophene units as D (electron-donating group)–π (π-conjugated bridge) moiety and the (D–π)2Ph-type fluorescent dye OTK-2 with the two D–π moieties connected through a phenyl ring were derived by oxidative homocoupling of a stannyl D–π unit and Stille coupling of a

• band, but also intense fluorescence emission both in solution and the solid state. Keywords: (D–π)2 structure; fluorescence; fluorescent dyes; photoabsorption; redox properties; Introduction The design and development of a new type of organic fluorescent dyes have been of considerable scientific and

Electrochemical and spectroscopic properties of twisted dibenzo[g,p]chrysene derivatives

• Tomoya Imai,
• Ryuhei Akasaka,
• Naruhiro Yoshida,
• Toru Amaya and
• Tetsuo Iwasawa

Beilstein J. Org. Chem. 2022, 18, 963–971, doi:10.3762/bjoc.18.96

• , a strong photoluminescence was observed for DBC-H and DBC-Si. Keywords: DFT calculation; dibenzo[g,p]chrysenes; fluorescent compounds; oxidation; polycyclic aromatic hydrocarbon (PAH); twisted acenes; Introduction Polycyclic aromatic hydrocarbons (PAHs) have attracted interest as potential

Introducing a new 7-ring fused diindenone-dithieno[3,2-b:2',3'-d]thiophene unit as a promising component for organic semiconductor materials

• Valentin H. K. Fell,
• Joseph Cameron,
• Alexander L. Kanibolotsky,
• Eman J. Hussien and
• Peter J. Skabara

Beilstein J. Org. Chem. 2022, 18, 944–955, doi:10.3762/bjoc.18.94

• (the basic unit of processors) [6], solar cells, and LEDs [7]. Inorganic compounds, e.g. III-V type inorganics are widely used, however, in recent years, organic molecules with semiconducting and fluorescent properties have emerged as an alternative with advantages such as solution processing [8][9][10

Morita–Baylis–Hillman reaction of 3-formyl-9H-pyrido[3,4-b]indoles and fluorescence studies of the products

• Nisha Devi and
• Virender Singh

Beilstein J. Org. Chem. 2022, 18, 926–934, doi:10.3762/bjoc.18.92

• . The present work is a step towards this and assimilates the results related to the exploration of 3-formyl-9H-β-carbolines for the synthesis of β-carboline C-3 substituted MBH adducts followed by evaluation of their fluorescent characteristic. The effect of contact time, solvent system, concentration

• relationships were concluded which are outlined in Figure 6. It was concluded from the structure–fluorescence activity relationships of C-3-substituted pyrido[3,4-b]indole derivatives that the products with o-bromophenyl substituent at R1 position (7cB and 7cE) were the most fluorescent derivatives among all

• . Also, substituted phenyl derivatives were more fluorescent than the dimethoxymethyl substituted derivatives 7aA–7aE. Further, it was observed that an ethyl substituent at N-9 position of β-carboline decreased the fluorescence intensity in 10eA–10eB than 7eD which is a N-unsubstituted derivative while

Post-synthesis from Lewis acid–base interaction: an alternative way to generate light and harvest triplet excitons

• Hengjia Liu and
• Guohua Xie

Beilstein J. Org. Chem. 2022, 18, 825–836, doi:10.3762/bjoc.18.83

• Guangdong Province, Shantou University, Shantou 518060, People’s Republic of China Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan 430074, People’s Republic of China 10.3762/bjoc.18.83 Abstract The changes in absorption and emission of fluorescent

• fluorescent materials containing Lewis basic nitrogen heterocycles are more likely to provide the feasible band gap modulation. The essence of such phenomenon originates from Lewis acid–base coordination and adducts, which highly depends on the electron-accepting property of the Lewis acids. This

• are fluorescent compounds. Based on the spin statistics, the fluorescent emitters can only use singlet excitons for light generation [5]. In contrast, phosphorescent materials based on metal complexes could achieve a high internal quantum efficiency (IQE) up to 100% through intersystem crossing (ISC