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Search for "thermal stability" in Full Text gives 236 result(s) in Beilstein Journal of Organic Chemistry. Showing first 200.

Thienothiophene-based organic light-emitting diode: synthesis, photophysical properties and application

  • Recep Isci and
  • Turan Ozturk

Beilstein J. Org. Chem. 2023, 19, 1849–1857, doi:10.3762/bjoc.19.137

Graphical Abstract
  • under N2 atmosphere (Figure 4). The initial mass loss (5%) around 120 °C could be due to residual water and/or solvent. The highest decomposition was observed at around 405 oC and 14% of DMB-TT-TPA (8) remained without ash up to 750 °C, indicating that the compound has an excellent thermal stability
  • . The high thermal stability is profitable for the preparation of stable and durable OLED devices. Computational chemistry Ground-state geometry optimization of DMB-TT-TPA (8) was performed using density functional theory (DFT) calculations with the Gaussian 16 software at the B3LYP/6-31G (d,p) level
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Published 07 Dec 2023

Charge carrier transport in perylene-based and pyrene-based columnar liquid crystals

  • Alessandro L. Alves,
  • Simone V. Bernardino,
  • Carlos H. Stadtlober,
  • Edivandro Girotto,
  • Giliandro Farias,
  • Rodney M. do Nascimento,
  • Sergio F. Curcio,
  • Thiago Cazati,
  • Marta E. R. Dotto,
  • Juliana Eccher,
  • Leonardo N. Furini,
  • Hugo Gallardo,
  • Harald Bock and
  • Ivan H. Bechtold

Beilstein J. Org. Chem. 2023, 19, 1755–1765, doi:10.3762/bjoc.19.128

Graphical Abstract
  • derivatives are among the most investigated due to their easy functionalization, high chemical and thermal stability, strong photoluminescence, and n-type semiconductor character. They tend to adopt columnar organization due to the strong π–π interaction of the rigid cores, providing a path for the efficient
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Published 16 Nov 2023

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

Graphical Abstract
  • morphology on Qx26 and Qx27, employing indacenodithiophene, Qx and rhodanine as donor, acceptor and end group, respectively. The incorporation of specific side chains facilitated improved thermal stability, solubility, and broad absorption spectra (300–750 nm), narrow bandgaps (1.68–1.74 eV) and PCEs in the
  • properties of Qx45 series by incorporating electron-donating (methyl) and electron-withdrawing groups (bromo and nitro) (Figure 6). The observation of low-lying LUMO levels (−3.29 to −3.43 eV) and thermal stability in these dyes suggested their potential as efficient ETMs [50]. Similarly, Singh et al
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Published 09 Nov 2023

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

Graphical Abstract
  • scanning calorimetry (DSC) under N2 atmosphere at a scanning rate of 10 °C min−1. As displayed in Figure 5a, the compound has a high thermal stability with a decomposition temperature at 5% weight loss (T5d) of 498 °C, a glass transition temperature (Tg) of 236 °C, and a melting temperature (Tm) of 376 °C
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Published 03 Nov 2023

A series of perylene diimide cathode interlayer materials for green solvent processing in conventional organic photovoltaics

  • Kathryn M. Wolfe,
  • Shahidul Alam,
  • Eva German,
  • Fahad N. Alduayji,
  • Maryam Alqurashi,
  • Frédéric Laquai and
  • Gregory C. Welch

Beilstein J. Org. Chem. 2023, 19, 1620–1629, doi:10.3762/bjoc.19.119

Graphical Abstract
  • transport, exhibit high thermal stability, are highly tunable in terms of their physical and chemical properties, and can be readily doped thereby increasing electronic conductivity. Some of the most widely used PDI materials for CILs are PDIN [14], PDINN [15], and PDINO (Figure 1a) [14][15]. Past work in
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Published 26 Oct 2023

Synthesis of 5-arylidenerhodanines in L-proline-based deep eutectic solvent

  • Stéphanie Hesse

Beilstein J. Org. Chem. 2023, 19, 1537–1544, doi:10.3762/bjoc.19.110

Graphical Abstract
  • promising emerging class of green solvents as they offer numerous advantages, such as low volatility, non-flammability, chemical and thermal stability, recyclability, and above all a good biodegradability [10]. Moreover, their synthesis is usually easy and cheap as DES are formed by simply mixing an H-bond
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Published 04 Oct 2023

Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review

  • Nosheen Beig,
  • Varsha Goyal and
  • Raj K. Bansal

Beilstein J. Org. Chem. 2023, 19, 1408–1442, doi:10.3762/bjoc.19.102

Graphical Abstract
  • the NHC–CuN(SiMe3)2 complexes 42, 45, and 48, respectively. All synthesized complexes were characterized by TGA to explain their thermal behavior. The impact of the N-allyl substituent and backbone character on volatility and thermal stability of the copper amides were investigated and it was found
  • that the saturated copper–carbene complexes exhibit a higher thermal stability as compared to the unsaturated copper–carbene complexes. In another interesting research paper, César et al., in 2015, reported the synthesis of the mesoionic 5-acetylimidazolium-4-olate 49 which served as a precursor for an
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Published 20 Sep 2023

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

Graphical Abstract
  • identical molecular peak ion and C, H, N values within acceptable deviation of 0.4%. The decomposition temperature (Td, corresponds to 5% weight loss) was measured by thermogravimetric analysis (TGA) indicating excellent thermal stability for 4BGIPN with Td = 425 °C, which is similar to the benchmark
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Published 07 Sep 2023

The effect of dark states on the intersystem crossing and thermally activated delayed fluorescence of naphthalimide-phenothiazine dyads

  • Liyuan Cao,
  • Xi Liu,
  • Xue Zhang,
  • Jianzhang Zhao,
  • Fabiao Yu and
  • Yan Wan

Beilstein J. Org. Chem. 2023, 19, 1028–1046, doi:10.3762/bjoc.19.79

Graphical Abstract
  • unit, the ECS state of the NI-PTZ-F-O, NI-PTZ-Ph-O, and NI-PTZ-C5-O was increased by ca. 0.8 eV. Thus, we do not expect TADF for these three dyads, especially in HEX. In polar solvents, such as ACN, no TADF was observed. Thermal stability analysis (thermogravimetry analysis, TGA) The thermal stability
  • % thermal weight loss) of each compound were determined as follows: NI-PTZ-F (422 °C), NI-PTZ-Ph (375 °C), NI-PTZ-CH3 (436 °C), NI-PTZ-OCH3 (432 °C), NI-PTZ-F-O (371 °C), NI-PTZ-Ph-O (362 °C), NI-PTZ-C5 (436 °C), NI-PTZ-C5-O (373 °C). The results show that the thermal stability of these compounds is
  • excellent, and the thermal stability of dyads containing unoxidized PTZ units is better than those containing oxidized PTZ units. Femtosecond transient absorption (fs-TA) spectra In order to study the CS, charge recombination (CR), and ISC of the compounds, the femtosecond transient spectra were studied
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Published 19 Jul 2023

Discrimination of β-cyclodextrin/hazelnut (Corylus avellana L.) oil/flavonoid glycoside and flavonolignan ternary complexes by Fourier-transform infrared spectroscopy coupled with principal component analysis

  • Nicoleta G. Hădărugă,
  • Gabriela Popescu,
  • Dina Gligor (Pane),
  • Cristina L. Mitroi,
  • Sorin M. Stanciu and
  • Daniel Ioan Hădărugă

Beilstein J. Org. Chem. 2023, 19, 380–398, doi:10.3762/bjoc.19.30

Graphical Abstract
  • complexes was kneading the components at various molar ratios (1:1:1 and 3:1:1 for β-CD hydrate:hazelnut oil (average molar mass of 900 g/mol):flavonoid). The recovering yields of the ternary complexes were in the range of 51.5–85.3% and were generally higher for the 3:1:1 samples. The thermal stability was
  • compounds [5]. The resulting supramolecular inclusion complexes provide enhanced water solubility and bioavailability/bioaccessibility of the nanoencapsulated bioactive compounds, higher oxidative and thermal stability or photostability of labile compounds, and their controlled release [6][7]. Vegetable oil
  • apparent water solubility and bioaccessibility of the oil and fat components. The oxidative stability of the polyunsaturated FA glycerides or free FAs is significantly increased by CD nanoencapsulation. Thus, a high thermal stability was obtained for linoleic acid encapsulated into α-CD by co
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Published 28 Mar 2023

Inclusion complexes of the steroid hormones 17β-estradiol and progesterone with β- and γ-cyclodextrin hosts: syntheses, X-ray structures, thermal analyses and API solubility enhancements

  • Alexios I. Vicatos,
  • Zakiena Hoossen and
  • Mino R. Caira

Beilstein J. Org. Chem. 2022, 18, 1749–1762, doi:10.3762/bjoc.18.184

Graphical Abstract
  • thermogravimetric analyses (TGA) and differential scanning calorimetry (DSC) analyses for the four CD inclusion complexes (Figure 5a–d) primarily indicated their water content and thermal stability, the data for their thermal events being summarised in Table 1. These results were further accompanied by hot stage
  • particular (Table 1). Thus, all CD complexes displayed thermal integrity until relatively high temperatures of at least 100 °C, prior to phase transitions and decomposition, indicating acceptable thermal stability for commercial pharmaceutical applications. Further analytical details regarding the TGA, dTGA
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Published 22 Dec 2022

1,4,6,10-Tetraazaadamantanes (TAADs) with N-amino groups: synthesis and formation of boron chelates and host–guest complexes

  • Artem N. Semakin,
  • Ivan S. Golovanov,
  • Yulia V. Nelyubina and
  • Alexey Yu. Sukhorukov

Beilstein J. Org. Chem. 2022, 18, 1424–1434, doi:10.3762/bjoc.18.148

Graphical Abstract
  • in an atypical +4 oxidation state [27][28][29]. Recently, TAAD was used to improve the thermal and photochemical stability of MAPbI3 perovskite films (most likely through coordination of Pb(II) ions) [30]. The disadvantages of 3O-TAADs, however, are limited thermal stability (due to cage opening to
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Published 11 Oct 2022
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  • 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
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Published 10 Oct 2022

Mechanochemical bottom-up synthesis of phosphorus-linked, heptazine-based carbon nitrides using sodium phosphide

  • Blaine G. Fiss,
  • Georgia Douglas,
  • Michael Ferguson,
  • Jorge Becerra,
  • Jesus Valdez,
  • Trong-On Do,
  • Tomislav Friščić and
  • Audrey Moores

Beilstein J. Org. Chem. 2022, 18, 1203–1209, doi:10.3762/bjoc.18.125

Graphical Abstract
  • broad Bragg reflections at 2θ = 16° and 28°. This suggests a high thermal stability of the g-h-PCN structure, being formed during the mild milling and aging conditions, with no need for annealing. X-ray photoelectron spectroscopy (XPS) To gain insight into the atomic speciation within the structure and
  • the pure reaction product. The variations may be ascribed to the oxygen content found by XPS (Figure 2) or that the mechanochemically synthesized material exists in a different spatial configuration to those previously predicted [46][47]. Thermal stability Prior to annealing, g-h-PCN was found to show
  • thermal stability upwards of 200 °C through TGA in nitrogen and air (Supporting Information File 1, Figures S6 and S7). The initial loss seen for both samples is attributed to surface-bound water and carbon dioxide. The g-h-PCN300 retains more mass to upwards of 400 °C in both air and nitrogen, however
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Published 12 Sep 2022

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

Graphical Abstract
  • ] and ease of tunability of properties [11]. Although their thermal stability is lower than their inorganic counterparts [12], their properties, e.g. the HOMO–LUMO gap, can be tailored and fine-tuned by molecular design [3]. Depending on their structure and/or functional groups, they can be designed for
  • its phase below its melting point. The limits of thermal stability were recorded by a 5% mass loss at elevated temperatures, as determined by thermal gravimetric analysis (TGA), and found to be 406 °C, indicating a high thermal stability (Figure S18 in Supporting Information File 1). Electrochemistry
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Published 01 Aug 2022

Comparative study of thermally activated delayed fluorescent properties of donor–acceptor and donor–acceptor–donor architectures based on phenoxazine and dibenzo[a,j]phenazine

  • Saika Izumi,
  • Prasannamani Govindharaj,
  • Anna Drewniak,
  • Paola Zimmermann Crocomo,
  • Satoshi Minakata,
  • Leonardo Evaristo de Sousa,
  • Piotr de Silva,
  • Przemyslaw Data and
  • Youhei Takeda

Beilstein J. Org. Chem. 2022, 18, 459–468, doi:10.3762/bjoc.18.48

Graphical Abstract
  • , where POZ-DBPHZ has the twice higher value which in total should give a much lower performance in the device for 1. Thermal stability To fabricate the OLED devices by thermal evaporation techniques, a high thermal stability is required. To evaluate the effect of the donor number on the thermal stability
  • deposition process. However, when compared with the D–A–D counterpart, the Td of 1 is much lower (by 111 °C) than that of POZ-DBPHZ (453 °C) [17]. These data would support that the increase in the sterically hindered donors in emitting molecule suppress intermolecular contact to enhance the thermal stability
  • , the one-less number of donor units in the molecular scaffold led to lower solubility in organic solvents and thermal stability, presumably due to the less steric hindrance around the π-extended conjugated acceptor unit with the unsymmetric molecule structure. The OLEDs fabricated with the D–A emitter
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Published 25 Apr 2022

Photophysical, photostability, and ROS generation properties of new trifluoromethylated quinoline-phenol Schiff bases

  • Inaiá O. Rocha,
  • Yuri G. Kappenberg,
  • Wilian C. Rosa,
  • Clarissa P. Frizzo,
  • Nilo Zanatta,
  • Marcos A. P. Martins,
  • Isadora Tisoco,
  • Bernardo A. Iglesias and
  • Helio G. Bonacorso

Beilstein J. Org. Chem. 2021, 17, 2799–2811, doi:10.3762/bjoc.17.191

Graphical Abstract
  • 4-substituted 4-methoxy-1,1,1-trifluoroalk-3-en-2-ones in a two-step reaction procedure and with satisfactory yields of up to 87%. The prepared 6-aminoquinolines presented promising photophysical properties and high thermal stability [14]. In this sense, the present study aimed to synthesize a novel
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Published 01 Dec 2021

In-depth characterization of self-healing polymers based on π–π interactions

  • Josefine Meurer,
  • Julian Hniopek,
  • Johannes Ahner,
  • Michael Schmitt,
  • Jürgen Popp,
  • Stefan Zechel,
  • Kalina Peneva and
  • Martin D. Hager

Beilstein J. Org. Chem. 2021, 17, 2496–2504, doi:10.3762/bjoc.17.166

Graphical Abstract
  • differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The TGA revealed a high thermal stability up to a temperature of 370 °C (for curves see Supporting Information File 1). The temperature was determined at a residual mass of 95%. The DSC on the other hand indicates several thermal
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Published 29 Sep 2021

Chemical syntheses and salient features of azulene-containing homo- and copolymers

  • Vijayendra S. Shetti

Beilstein J. Org. Chem. 2021, 17, 2164–2185, doi:10.3762/bjoc.17.139

Graphical Abstract
  • subjected to the oxidative polymerization by using ferric chloride to obtain polymers 33–38 in 42–58% yields as shown in Scheme 8. These polymers possessed good thermal stability (Td > 400 °C) and most of them were soluble in organic solvents such as THF, chloroform, dichloromethane, xylene, and toluene
  • -dibromo-6-(n-dodecyl)azulene (13) with 2,5-bis(trimethylstannyl)thiophene (44) under Stille reaction conditions produced the polymer 45 in 62% yield (Scheme 10). The Mn and PDI for polymer 45 were 5100 Da and 1.4, respectively and its thermal stability was excellent (Td = 404 °C). Polymer 45 exhibited
  • , and 56 displayed good solubility in most of the commonly used organic solvents and GPC analysis revealed their number-average molecular weight (Mn) to be in the range of 25800 to 48600 Da with polydispersity in the range 1.29–1.9. They also exhibited excellent thermal stability as indicated by their
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Published 24 Aug 2021

Cationic oligonucleotide derivatives and conjugates: A favorable approach for enhanced DNA and RNA targeting oligonucleotides

  • Mathias B. Danielsen and
  • Jesper Wengel

Beilstein J. Org. Chem. 2021, 17, 1828–1848, doi:10.3762/bjoc.17.125

Graphical Abstract
  • ][40][41]. The structures of some of the uridine derivatives are shown in Table 1. In general, the attachment of amine-functionalized groups on the pyrimidine C-5 position positively affects both the thermal stability and the nuclease resistance of the resulting amine-modified ONs. A tris-aminated
  • significant improvement in Tm was observed when the functionalizing groups were changed from ethylenediamine to either trimethylenediamine (monomer 42) or putrescine (monomer 43), demonstrating that the length between the cationic amino group and the sugar scaffold is important for the thermal stability
  • giving the best stabilization (up to 5.7 °C for four incorporations in an 18-mer ON relative to the control), whereas all gave similar and/or decreased thermal stability against RNA relative to the natural control ON [97]. It is noteworthy to mention that all monomers allowed the design of ASOs that were
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Published 29 Jul 2021

Development of N-F fluorinating agents and their fluorinations: Historical perspective

  • Teruo Umemoto,
  • Yuhao Yang and
  • Gerald B. Hammond

Beilstein J. Org. Chem. 2021, 17, 1752–1813, doi:10.3762/bjoc.17.123

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Published 27 Jul 2021

Chemical approaches to discover the full potential of peptide nucleic acids in biomedical applications

  • Nikita Brodyagin,
  • Martins Katkevics,
  • Venubabu Kotikam,
  • Christopher A. Ryan and
  • Eriks Rozners

Beilstein J. Org. Chem. 2021, 17, 1641–1688, doi:10.3762/bjoc.17.116

Graphical Abstract
  • ]. Interestingly and in contrast to other backbone-constrained PNAs, pyrrolidinyl α/β-dipeptide PNA formed PNA–DNA complexes having higher thermal stability compared to PNA–RNA complexes [63][64]. Most likely, the one atom longer PNA backbone, which is rigidified and preorganized by cyclic moieties, may align
  • precursors in vitro [133]. Furan (F, Figure 8) as a reactive nucleobase mimic was well accommodated in a duplex with DNA without decreasing its thermal stability [134]. Upon oxidation of the furan ring, F-modified PNAs reacted preferentially with cytosine and adenine and irreversibly crosslinked with ssDNA
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Published 19 Jul 2021

Recent advances in the application of isoindigo derivatives in materials chemistry

  • Andrei V. Bogdanov and
  • Vladimir F. Mironov

Beilstein J. Org. Chem. 2021, 17, 1533–1564, doi:10.3762/bjoc.17.111

Graphical Abstract
  • polymer with an effective ratio μh/μe = 3.94 cm2⋅V−1⋅s−1/3.50 cm2⋅V−1⋅s−1. Recently, diketopyrrolo[3,4-c]pyrrole (DPP) derivatives, which are highly conjugated electron-withdrawing heterocycles with high charge conductivity, broad absorption spectrum, photostability, and thermal stability have attracted
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Published 06 Jul 2021

Double-headed nucleosides: Synthesis and applications

  • Vineet Verma,
  • Jyotirmoy Maity,
  • Vipin K. Maikhuri,
  • Ritika Sharma,
  • Himal K. Ganguly and
  • Ashok K. Prasad

Beilstein J. Org. Chem. 2021, 17, 1392–1439, doi:10.3762/bjoc.17.98

Graphical Abstract
  • group (Scheme 32) [71]. The double-headed nucleoside monomer 5′-O-(4,4′-dimethoxytrityl)-5-(thymin-1-yl)methyl-2′-deoxyuridine (130) was converted into the corresponding phosphoramidite at the C-3′-hydroxy group and then incorporated into oligonucleotides and was found to decrease the thermal stability
  • phosphoramidites and then introduced into oligonucleotides. The thermal stability of DNA:DNA and DNA:RNA duplexes was determined and it was found that duplexes with a meta-substitution and a phenylacetylene linker were more stable than the corresponding para-substituted and phenyl-linker containing derivatives
  • treatment with methanolic ammonia and DMA–DMF (Scheme 37) [71]. Both double-headed nucleoside monomers 143 and 146 were phosphoramidated at the C-3′ hydroxy group and incorporated into oligonucleotides. The synthesized oligonucleotides were found to decrease the thermal stability of the duplexes. However
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Published 08 Jun 2021
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  • interdisciplinary interest from both fundamental as well as applied viewpoint on account of their wonderful optoelectronic properties. The scientific interest in two-dimensional star-shaped PAHs particularly in truxene architectures arises because of their high thermal stability, exceptional solubility and ease
  • ]. More interestingly, the high fluorescence quantum yield as well as the excellent photoluminescence quantum efficiency in addition to extraordinary thermal stability are the most significant characteristics of these systems. Interestingly, this versatile C3-symmetric aromatic framework can also formally
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Published 02 Jun 2021
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