Synthesis of esters of diaminotruxillic bis-amino acids by Pd-mediated photocycloaddition of analogs of the Kaede protein chromophore

• Esteban P. Urriolabeitia,
• Pablo Sánchez,
• Alexandra Pop,
• Cristian Silvestru,
• Eduardo Laga,
• Ana I. Jiménez and
• Carlos Cativiela

Beilstein J. Org. Chem. 2020, 16, 1111–1123, doi:10.3762/bjoc.16.98

• precursors of the photoconvertible chromophore of the Kaede protein, an imidazolone with outstanding photophysical properties [31][32][33][34][35][36][37][38]. It is clear from Figure 2b that the molecular skeleton contains different reactive functional groups, which offer a variety of structural

Synthesis of novel multifunctional carbazole-based molecules and their thermal, electrochemical and optical properties

• Nuray Altinolcek,
• Ahmet Battal,
• Mustafa Tavasli,
• William J. Peveler,
• Holly A. Yu and
• Peter J. Skabara

Beilstein J. Org. Chem. 2020, 16, 1066–1074, doi:10.3762/bjoc.16.93

• component), whereas the link by conjugation between the same functionalities in 7a is missing. The resulting stronger ICT component in 7b explains the big difference in photophysical properties. Experimental All reagents were standard reagent grade and purchased from Sigma-Aldrich, Merck and Alfa Aesar

Aryl-substituted acridanes as hosts for TADF-based OLEDs

• Naveen Masimukku,
• Dalius Gudeika,
• Oleksandr Bezvikonnyi,
• Ihor Syvorotka,
• Rasa Keruckiene,
• Dmytro Volyniuk and
• Juozas V. Grazulevicius

Beilstein J. Org. Chem. 2020, 16, 989–1000, doi:10.3762/bjoc.16.88

• molecular weights resulting in a stronger intermolecular interaction and by larger volumes restricting molecular motion. These observations confirm that compounds 3–5 can be used for the preparation of thin amorphous layers on substrates. Photophysical properties The absorption and photoluminescence (PL

Aldehydes as powerful initiators for photochemical transformations

• Maria A. Theodoropoulou,
• Nikolaos F. Nikitas and
• Christoforos G. Kokotos

Beilstein J. Org. Chem. 2020, 16, 833–857, doi:10.3762/bjoc.16.76

• ) aldehydes have as photoinitiators. The photophysical properties and photoreactivity of benzaldehyde are initially provided, followed by applications of aldehydes as initiators for polymerization reactions. Finally, the applications to date regarding aldehydes as photoinitiators in organic synthesis are

• are useful photocatalysts, the corresponding aldehydes are not so widely utilized to promote chemical reactions. In this review, our goal was to summarize the photophysical properties of aromatic aldehydes, highlight the use of aldehydes as photoinitiators in polymerization reactions, and provide all

• examples where aldehydes were employed as photoinitiators in organic synthesis. Review Photophysical properties of carbonyl compounds The interest in the interaction of aldehydes with light to promote reactions can be traced many years back. In 1966, Davies and co-worker studied the energy transfer from

One-pot synthesis of dicyclopenta-fused peropyrene via a fourfold alkyne annulation

• Ji Ma,
• Yubin Fu,
• Junzhi Liu and
• Xinliang Feng

Beilstein J. Org. Chem. 2020, 16, 791–797, doi:10.3762/bjoc.16.72

• pentagons could be realized [11][12][13][14][15][16][17]. Among them, the cyclopenta-fused pyrenes are an important class of CP-PAHs owing to their unique physical and photophysical properties, such as high electron affinities and anomalous fluorescence [17][18][19][20]. However, the reported synthetic

Towards triptycene functionalization and triptycene-linked porphyrin arrays

• Gemma M. Locke,
• Keith J. Flanagan and
• Mathias O. Senge

Beilstein J. Org. Chem. 2020, 16, 763–777, doi:10.3762/bjoc.16.70

• and electrochemical properties of the porphyrins by increasing the size of the aromatic π-system [16]. In contrast, our approach described herein deviates significantly from previous studies by examining how isolating the individual porphyrin units affects the overall photophysical properties of the

• properties of triptycene complexes The photophysical properties of the five new triptycene-liked porphyrin/BODIPY compounds 7, 9, 14, 16 and 18 were investigated in preliminary studies for their suitability as model compounds for electron transfer in the context of artificial photosynthesis. Similar Soret

Synthesis of C₇₀-fragment buckybowls bearing alkoxy substituents

• Yumi Yakiyama,
• Shota Hishikawa and
• Hidehiro Sakurai

Beilstein J. Org. Chem. 2020, 16, 681–690, doi:10.3762/bjoc.16.66

• hydrogen bonds (C37∙∙∙O1, C11∙∙∙O2, C40∙∙∙O4) (Figure 5c). Photophysical properties of the dialkoxides were investigated by UV–vis and emission spectroscopies (Figure 6). UV–vis spectra of 5a and 5b well reflected the electric property of 1, showing two strong bands observed at around 280–300 nm and 330

Direct borylation of terrylene and quaterrylene

• Haruka Kano,
• Keiji Uehara,
• Kyohei Matsuo,
• Hironobu Hayashi,
• Hiroko Yamada and
• Naoki Aratani

Beilstein J. Org. Chem. 2020, 16, 621–627, doi:10.3762/bjoc.16.58

• photophysical properties of TB4 are also unchanged by the substituents because the carbon atoms at 2,5,10,13-positions have less coefficients on its HOMO and LUMO, estimated by theoretical calculations. Finally, the same borylation reaction was applied for quaterrylene, resulting in the formation of soluble

Regioselectively α- and β-alkynylated BODIPY dyes via gold(I)-catalyzed direct C–H functionalization and their photophysical properties

• Takahide Shimada,
• Shigeki Mori,
• Masatoshi Ishida and
• Hiroyuki Furuta

Beilstein J. Org. Chem. 2020, 16, 587–595, doi:10.3762/bjoc.16.53

• . Depending on the position of the ethynyl substituent in the BODIPY skeleton, the photophysical properties of the resulting α- and β-substituted BODIPYs are notably altered. The lowest S0–S1 transition absorbance and fluorescence bands are both bathochromically shifted as the number of substituents increases

• , while the emission quantum yields of the β-ethynylated derivatives are significantly lower than those of α-ethynylated ones. The current method should be useful for fine-tuning of the photophysical properties of BODIPY dyes as well as for constructing BODIPY-based building cores for functional π

• afford α-monoethynyl and α,α'-diethynyl-substituted BODIPYs 3 and 4, respectively. The resulting ethynylated BODIPY isomers demonstrated site-dependent photophysical properties. Results and Discussion Synthesis and characterization To prepare the α,α'-diethynyl BODIPY 4a, 5-mesityldipyrromethane 2 was

Copper-catalyzed remote C–H arylation of polycyclic aromatic hydrocarbons (PAHs)

• Anping Luo,
• Min Zhang,
• Zhangyi Fu,
• Jingbo Lan,
• Di Wu and
• Jingsong You

Beilstein J. Org. Chem. 2020, 16, 530–536, doi:10.3762/bjoc.16.49

• fluorescence, and have been widely applied in many scientific areas including chemistry, biomedicine and materials science [1][2][3][4][5][6]. The arylation reaction of PAHs is an important strategy to further extend the π-conjugation length, which can effectively adjust the photophysical properties of

• the C8–Cu bond delivers Cu(I), meantime, the OTf anion takes away the proton from the C7-position, affording the desired product 3 or 4. Subsequently, the photophysical properties of the arylation products 4k, 4n and 4o were investigated (Figure 1). Their absorption bands cover from 300 nm to 400 nm

Six-fold C–H borylation of hexa-peri-hexabenzocoronene

• Mai Nagase,
• Kenta Kato,
• Akiko Yagi,
• Yasutomo Segawa and
• Kenichiro Itami

Beilstein J. Org. Chem. 2020, 16, 391–397, doi:10.3762/bjoc.16.37

• 50% probability; all hydrogen atoms and solvent molecules (pentane) are omitted for clarity; gray: carbon; olive green: boron; red: oxygen. (b) Side view of 1. (c) Packing mode of 1. Photophysical properties of 1. (a) UV–vis absorption (solid lines) spectra, fluorescence (dotted line) spectrum

Synthesis and circularly polarized luminescence properties of BINOL-derived bisbenzofuro[2,3-b:3’,2’-e]pyridines (BBZFPys)

• Ryo Takishima,
• Yuji Nishii,
• Tomoaki Hinoue,
• Yoshitane Imai and
• Masahiro Miura

Beilstein J. Org. Chem. 2020, 16, 325–336, doi:10.3762/bjoc.16.32

• ; palladium; Introduction Densely-fused (hetero)aromatic compounds have been a key motif in a wide range of manufactured functional molecules, as they exhibit fundamentally useful electrochemical and photophysical properties. Considerable effort has therefore taken into the development of efficient methods

Recent developments in photoredox-catalyzed remote ortho and para C–H bond functionalizations

• Rafia Siddiqui and
• Rashid Ali

Beilstein J. Org. Chem. 2020, 16, 248–280, doi:10.3762/bjoc.16.26

• into chemical energy via the generation of reactive intermediates through electron transfer reactions. A photochemical reaction is directed by the photophysical properties of an electronically excited molecule. The first vibrational equilibrated singlet excited state is S1, and it depends on both

Reversible photoswitching of the DNA-binding properties of styrylquinolizinium derivatives through photochromic [2 + 2] cycloaddition and cycloreversion

• Sarah Kölsch,
• Heiko Ihmels,
• Jochen Mattay,
• Norbert Sewald and
• Brian O. Patrick

Beilstein J. Org. Chem. 2020, 16, 111–124, doi:10.3762/bjoc.16.13

• the alkene protons (3JH–H = 16 Hz) [70]. Absorption and emission properties The photophysical properties of the styrylquinolizinium derivatives 3a and 3c have already been reported [69], while the ones of 3b and 3d were determined in this work (Table 1 and Figure 1). In acetonitrile, the derivatives

Starazo triple switches – synthesis of unsymmetrical 1,3,5-tris(arylazo)benzenes

• Andreas H. Heindl and
• Hermann A. Wegner

Beilstein J. Org. Chem. 2020, 16, 22–31, doi:10.3762/bjoc.16.4

• 20% was achieved, whereas the methoxy derivative 3b could be isolated in a good yield of 59%. Having both tris(arylazo)benzenes 3a/3b in hand, UV–vis spectroscopy was used for preliminary investigations on the photophysical properties of the molecular triple switches 3. Both tris(arylazo)benzenes 3a

Synthesis and optoelectronic properties of benzoquinone-based donor–acceptor compounds

• Daniel R. Sutherland,
• Nidhi Sharma,
• Georgina M. Rosair,
• Ifor D. W. Samuel,
• Ai-Lan Lee and
• Eli Zysman-Colman

Beilstein J. Org. Chem. 2019, 15, 2914–2921, doi:10.3762/bjoc.15.285

• LUMO energies of 2–5 are in good agreement with the calculated values (Figure 3). Photophysical properties We next investigated the photophysical properties of 2–5. The UV–vis absorption and photoluminescence (PL) spectra in degassed DCM solution are shown in Figure 5, and the data are summarized in

• theoretical, electrochemical, and photophysical properties of the donor–acceptor compounds 2–5 were determined in solution and thin film. While compounds 2, 4, and 5 were very poorly emissive, 3 showed a green emission with a biexponential lifetime characterized by a prompt nanosecond component and a delayed

Design, synthesis and investigation of water-soluble hemi-indigo photoswitches for bioapplications

• Daria V. Berdnikova

Beilstein J. Org. Chem. 2019, 15, 2822–2829, doi:10.3762/bjoc.15.275

• . Photochemical and photophysical properties of hemi-indigo derivatives 1a–c and 2 in water. Supporting Information Supporting Information File 610: Additional spectral data, detailed description of the experiments performed, NMR of compounds Z-1a–c and LED characteristics. Acknowledgements This project has

Chemical tuning of photoswitchable azobenzenes: a photopharmacological case study using nicotinic transmission

• Lorenzo Sansalone,
• Jun Zhao,
• Matthew T. Richers and
• Graham C. R. Ellis-Davies

Beilstein J. Org. Chem. 2019, 15, 2812–2821, doi:10.3762/bjoc.15.274

• preserving all the favorable photophysical properties of the parent 4FAB scaffold, however, the tetrafluoro motif can significantly perturb pharmacophore–protein interactions. In contrast, we found that the freely diffusible 4FABTA probe could be pre-set with green light into an OFF state that was

Fluorinated maleimide-substituted porphyrins and chlorins: synthesis and characterization

• Valentina A. Ol’shevskaya,
• Elena G. Kononova and
• Andrei V. Zaitsev

Beilstein J. Org. Chem. 2019, 15, 2704–2709, doi:10.3762/bjoc.15.263

• the maleimide group with its rich biological activity to the tetrapyrrole macrocycles with their unique photophysical properties may result in new conjugates with improved chemical, biological and anticancer characteristics [28]. Moreover, maleimide is a stable functionality that rapidly and

Emission solvatochromic, solid-state and aggregation-induced emissive α-pyrones and emission-tuneable 1H-pyridines by Michael addition–cyclocondensation sequences

• Natascha Breuer,
• Irina Gruber,
• Christoph Janiak and
• Thomas J. J. Müller

Beilstein J. Org. Chem. 2019, 15, 2684–2703, doi:10.3762/bjoc.15.262

• , dimethylamino-substituted α-pyrones, as donor–acceptor systems, display remarkable photophysical properties, such as strongly red-shifted absorption and emission maxima with daylight fluorescence and fluorescence quantum yields up to 99% in solution and around 11% in the solid state, as well as pronounced

• achieved [4]. Small molecule organic fluorophores are particularly advantageous due to the potential of a tailored fine-tuning of their photophysical properties through synthetic modifications [5]. Based on their structural features, functionalized organic chromophores, containing N-, O- or S-atoms, are

• Supporting Information File 1) [50][51][52][53][54][55][56][57]. Photophysical properties Photophysical properties of 1H-pyridines 5 and 8 1H-Pyridine derivatives 5 are yellow or orange compounds under daylight (Figure 3, top) and fluoresce in solution (Figure 3, center) and in the solid state (Figure 3

Plasma membrane imaging with a fluorescent benzothiadiazole derivative

• Pedro H. P. R. Carvalho,
• Jose R. Correa,
• Karen L. R. Paiva,
• Daniel F. S. Machado,
• Jackson D. Scholten and
• Brenno A. D. Neto

Beilstein J. Org. Chem. 2019, 15, 2644–2654, doi:10.3762/bjoc.15.257

• -soluble and selective bioprobe for plasma membrane imaging. The new compound was efficiently synthesized in a two-step procedure with good yields. The photophysical properties were evaluated and the dye proved to have an excellent photostability in several solvents. DFT calculations were found in

• derivative. The photophysical properties of the new compound BTDE-4APTEG have been investigated and the results are summarized in Table 1 and presented in Figure 2. All absorption maxima were observed in the UV region close to 375 nm and with reasonable molar extinction coefficients. Large Stokes shifts were

• yielded the best overall performance across all studied solvents with an absolute deviation below 10 nm. PBE1PBE was therefore selected as the most suitable XCF (amongst the six investigated XCFs) for studying the photophysical properties of BTD-4APTEG. The structure geometry was fully optimized in

Arylisoquinoline-derived organoboron dyes with a triaryl skeleton show dual fluorescence

• Vânia F. Pais,
• Tristan Neumann,
• Ignacio Vayá,
• M. Consuelo Jiménez,
• Abel Ros and
• Uwe Pischel

Beilstein J. Org. Chem. 2019, 15, 2612–2622, doi:10.3762/bjoc.15.254

• advantageous photophysical properties that include spectrally tunable and highly intense fluorescence [1][2]. On the one hand, those compounds that contain the boron atom in a valence-saturated situation corresponding to sp3 hybridization (such as Bodipy dyes [3][4], N,C-chelate organoboron dyes [5][6][7][8][9

• electron-transfer phenomena or two-photon absorption [32][33][34][35][36]. As part of our research program we have developed arylisoquinolines that integrate a boronic acid ester [37][38][39] or a BMes2 unit [6][40]. The presence of the boron-substituent confers interesting photophysical properties to

• the verification of the effect of aromatic conjugation (naphthyl, anthryl, pyrenyl) and electron-donor strength (naphthyl versus 4-methoxynaphthyl) on the photophysical properties. Beside the observation of interesting dual emission properties for these dyes, some showed a pronounced ratiometric

Probing of local polarity in poly(methyl methacrylate) with the charge transfer transition in Nile red

• Aydan Yadigarli,
• Qimeng Song,
• Sergey I. Druzhinin and
• Holger Schönherr

Beilstein J. Org. Chem. 2019, 15, 2552–2562, doi:10.3762/bjoc.15.248

• substrate-supported ultrathin films [13], the analysis of the photophysical properties of tracer dye molecules was found to be beneficial. In time-resolved fluorescence measurements and dye diffusion studies, the nanoenvironments in polymersomes could be assigned [1][12], solute transport be characterized

Self-assembled coordination thioether silver(I) macrocyclic complexes for homogeneous catalysis

• Zhen Cao,
• Aline Lacoudre,
• Cybille Rossy and
• Brigitte Bibal

Beilstein J. Org. Chem. 2019, 15, 2465–2472, doi:10.3762/bjoc.15.239

• ). Finally, the photophysical properties of ligand syn-1 (20 μM) and complexes 1a–d (30 μM) were evaluated in dichloromethane (Supporting Information File 1, Figures S4–S8). The UV–visible and fluorescence emission spectra (λexc = 345 nm) of ligand and complexes were similar and correspond to those of 9,10

Synthesis of a dihalogenated pyridinyl silicon rhodamine for mitochondrial imaging by a halogen dance rearrangement

• Jessica Matthias,
• Thines Kanagasundaram,
• Klaus Kopka and
• Carsten S. Kramer

Beilstein J. Org. Chem. 2019, 15, 2333–2343, doi:10.3762/bjoc.15.226

• photophysical properties of numerous silicon rhodamines leading to further insights into the correlation of the dyes’ chemical structure with their fluorogenic behavior [27]. Regarding the quantum yield, Hanaoka et al. have shown that introduction of methyl, methoxy or dimethylamine groups into the benzene

• experiments (supported by DFT calculations) on the orbital effects of both halogens and the nitrogen position in the pyridine ring are needed to explain these effects with confidence. In addition, our SiR dye 15 displays photophysical properties (extinction coefficient, quantum yield, lifetime) in the same