Articles de revues : « Acceptor Systems »

1

Zhang, Deqing, et Martin Heeney. « Organic Donor–Acceptor Systems ». Asian Journal of Organic Chemistry 9, n^o 9 (septembre 2020) : 1251. http://dx.doi.org/10.1002/ajoc.202000465.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

2

Kotowicz, Sonia, Mateusz Korzec, Agnieszka Katarzyna Pająk, Sylwia Golba, Jan Grzegorz Małecki, Mariola Siwy, Justyna Grzelak, Sebastian Maćkowski et Ewa Schab-Balcerzak. « New Acceptor–Donor–Acceptor Systems Based on Bis-(Imino-1,8-Naphthalimide) ». Materials 14, n^o 11 (21 mai 2021) : 2714. http://dx.doi.org/10.3390/ma14112714.

Texte intégral

Résumé :

In this paper, six novel symmetrical bis-(imino-1,8-naphthalimides) differing in core and N-substituent structure were synthesized, and their thermal (TGA, DSC), optical (UV-Vis, PL), electrochemical (DPV, CV) properties were evaluated. The compounds were stable to 280 °C and could be transferred into amorphous materials. Electrochemical investigations showed their ability to occur reductions and oxidations processes. They exhibited deep LUMO levels of about −3.22 eV and HOMO levels above −5.80 eV. The optical investigations were carried out in the solutions (polar and non-polar) and in films and blends with PVK:PBD. Bis-(imino-1,8-naphthalimides) absorbed electromagnetic radiation in the range of 243–415 nm and emitted light from blue to yellow. Their capacity for light emission under voltage was preliminarily tested in devices with an active layer consisting of a neat compound and a blend with PVK:PBD. The diodes emitted green or red light.

Styles APA, Harvard, Vancouver, ISO, etc.

3

Pilarczyk, K., K. Lewandowska, K. Mech, M. Kawa, M. Gajewska, B. Barszcz, A. Bogucki, A. Podborska et K. Szaciłowski. « Charge transfer tuning in TiO2 hybrid nanostructures with acceptor–acceptor systems ». Journal of Materials Chemistry C 5, n^o 9 (2017) : 2415–24. http://dx.doi.org/10.1039/c6tc05190a.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

4

Pop, Flavia, et Narcis Avarvari. « Covalent non-fused tetrathiafulvalene–acceptor systems ». Chemical Communications 52, n^o 51 (2016) : 7906–27. http://dx.doi.org/10.1039/c6cc01827k.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

5

Ignat'ev, N., L. Netchitaylo, R. Garlyauskaite et L. Yagupolskii. « Electrochemical reduction of super-acceptor systems ». Journal of Fluorine Chemistry 58, n^o 2-3 (août 1992) : 280. http://dx.doi.org/10.1016/s0022-1139(00)80736-8.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

6

Im, C., W. Tian, H. Bässler, A. Fechtenkötter, M. D. Watson et K. Müllen. « Photoconduction in organic donor–acceptor systems ». Journal of Chemical Physics 119, n^o 7 (15 août 2003) : 3952–57. http://dx.doi.org/10.1063/1.1590954.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

7

Zych, Dawid, et Aneta Slodek. « Acceptor-π-Acceptor-Acceptor/Donor systems containing dicyanovinyl acceptor group with substituted 1,2,3-triazole motif – synthesis, photophysical and theoretical studies ». Journal of Molecular Structure 1204 (mars 2020) : 127488. http://dx.doi.org/10.1016/j.molstruc.2019.127488.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

8

Maiya, G. Bhaskar, et V. Krishnan. « Intramolecular electron transfer in donor-acceptor systems. Porphyrins bearing trinitroaryl acceptor group ». Journal of Physical Chemistry 89, n^o 24 (novembre 1985) : 5225–35. http://dx.doi.org/10.1021/j100270a022.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

9

Duan, Pengfei, Deepak Asthana, Takuya Nakashima, Tsuyoshi Kawai, Nobuhiro Yanai et Nobuo Kimizuka. « All-or-none switching of photon upconversion in self-assembled organogel systems ». Faraday Discussions 196 (2017) : 305–16. http://dx.doi.org/10.1039/c6fd00170j.

Texte intégral

Résumé :

Aggregation-induced photon upconversion (iPUC) based on a triplet–triplet annihilation (TTA) process is successfully developed via controlled self-assembly of donor–acceptor pairs in organogel nanoassemblies. Although segregation of donor from acceptor assemblies has been an outstanding problem in TTA-based UC and iPUC, we resolved this issue by modifying both the triplet donor and aggregation induced emission (AIE)-type acceptor with glutamate-based self-assembling moieties. These donors and acceptors co-assemble to form organogels without segregation. Interestingly, these donor–acceptor binary gels show upconversion at room temperature but the upconversion phenomena were lost upon dissolution of the gels on heating. The observed changes in TTA-UC emission were thermally reversible, reflecting the controlled assembly/disassembly of the binary molecular systems. The observed on/off ratio of UC emission was much higher than that of the aggregation-induced fluorescence of the acceptor, which highlights the important role of iPUC, i.e., multi-exciton TTA for photoluminescence switching. This work bridges iPUC and supramolecular chemistry and provides a new strategy for designing stimuli-responsive upconversion systems.

Styles APA, Harvard, Vancouver, ISO, etc.

10

DelPo, Courtney A., Saeed-Uz-Zaman Khan, Kyu Hyung Park, Bryan Kudisch, Barry P. Rand et Gregory D. Scholes. « Polariton Decay in Donor–Acceptor Cavity Systems ». Journal of Physical Chemistry Letters 12, n^o 40 (1 octobre 2021) : 9774–82. http://dx.doi.org/10.1021/acs.jpclett.1c02644.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

11

Leikauf, B., H. A. Schneider et W. Regel. « Electron-donor-acceptor interactions with cellulosic systems ». Polymer Bulletin 22, n^o 5-6 (décembre 1989) : 573–78. http://dx.doi.org/10.1007/bf00718936.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

12

Das, Paramita, Ray J. Butcher et Chhanda Mukhopadhyay. « ChemInform Abstract : Zinc Titanate Nanopowder : An Advanced Nanotechnology Based Recyclable Heterogeneous Catalyst for the One-Pot Selective Synthesis of Self-Aggregated Low-Molecular Mass Acceptor-Donor-Acceptor-Acceptor Systems and Acceptor-Donor-Accepto ». ChemInform 43, n^o 39 (30 août 2012) : no. http://dx.doi.org/10.1002/chin.201239045.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

13

Kournoutas, Fotis, Kostas Seintis, Nikolaos Karakostas, Jiří Tydlitát, Sylvain Achelle, George Pistolis, Filip Bureš et Mihalis Fakis. « Photophysical and Protonation Time Resolved Studies of Donor–Acceptor Branched Systems With Pyridine Acceptors ». Journal of Physical Chemistry A 123, n^o 2 (26 octobre 2018) : 417–28. http://dx.doi.org/10.1021/acs.jpca.8b08628.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

14

Im, Chan, Sang-Woong Kang, Jeong-Yoon Choi et Jongdeok An. « Comparing Donor- and Acceptor-Originated Exciton Dynamics in Non-Fullerene Acceptor Blend Polymeric Systems ». Polymers 13, n^o 11 (28 mai 2021) : 1770. http://dx.doi.org/10.3390/polym13111770.

Texte intégral

Résumé :

Non-fullerene type acceptors (NFA) have gained attention owing to their spectral extension that enables efficient solar energy capturing. For instance, the solely NFA-mediated absorbing region contributes to the photovoltaic power conversion efficiency (PCE) as high as ~30%, in the case of the solar cells comprised of fluorinated materials, PBDB-T-2F and ITIC-4F. This implies that NFAs must be able to serve as electron donors, even though they are conventionally assigned as electron acceptors. Therefore, the pathways of NFA-originated excitons need to be explored by the spectrally resolved photovoltaic characters. Additionally, excitation wavelength dependent transient absorption spectroscopy (TAS) was performed to trace the nature of the NFA-originated excitons and polymeric donor-originated excitons separately. Unique origin-dependent decay behaviors of the blend system were found by successive comparing of those solutions and pristine films which showed a dramatic change upon film formation. With the obtained experimental results, including TAS, a possible model describing origin-dependent decay pathways was suggested in the framework of reaction kinetics. Finally, numerical simulations based on the suggested model were performed to verify the feasibility, achieving reasonable correlation with experimental observables. The results should provide deeper insights in to renewable energy strategies by using novel material classes that are compatible with flexible electronics.

Styles APA, Harvard, Vancouver, ISO, etc.

15

Çakal, Deniz, Yalçın Boztaş, Akın Akdag et Ahmet M. Önal. « Investigation of Fluorine Atom Effect on Benzothiadiazole Acceptor Unit in Donor Acceptor Donor Systems ». Journal of The Electrochemical Society 166, n^o 12 (2019) : G141—G147. http://dx.doi.org/10.1149/2.0471912jes.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

16

Ohtani, Shunsuke, Masayuki Gon, Kazuo Tanaka et Yoshiki Chujo. « Construction of the Luminescent Donor–Acceptor Conjugated Systems Based on Boron-Fused Azomethine Acceptor ». Macromolecules 52, n^o 9 (24 avril 2019) : 3387–93. http://dx.doi.org/10.1021/acs.macromol.9b00259.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

17

Bergkamp, Jesse J., Silvio Decurtins et Shi-Xia Liu. « Current advances in fused tetrathiafulvalene donor–acceptor systems ». Chemical Society Reviews 44, n^o 4 (2015) : 863–74. http://dx.doi.org/10.1039/c4cs00255e.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

18

Fischer, Markus K. R., Chang-Qi Ma, René A. J. Janssen, Tony Debaerdemaeker et Peter Bäuerle. « Core-functionalized dendritic oligothiophenes—novel donor–acceptor systems ». Journal of Materials Chemistry 19, n^o 27 (2009) : 4784. http://dx.doi.org/10.1039/b904243a.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

19

Albinsson, Bo, et Jerker Mårtensson. « Excitation energy transfer in donor–bridge–acceptor systems ». Physical Chemistry Chemical Physics 12, n^o 27 (2010) : 7338. http://dx.doi.org/10.1039/c003805a.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

20

Sneddon, Scott F., et Charles L. Brooks. « The conformations of proline-linked donor-acceptor systems ». Journal of the American Chemical Society 114, n^o 21 (octobre 1992) : 8220–25. http://dx.doi.org/10.1021/ja00047a036.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

21

Mews, Rüdiger. « Donor-acceptor properties of sulphur-nitrogen-fluorine systems ». Journal of Fluorine Chemistry 29, n^o 1-2 (août 1985) : 21. http://dx.doi.org/10.1016/s0022-1139(00)83256-x.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

22

Li, Zhen, Mengyuan He, Dangdang Xu et Zhihong Liu. « Graphene materials-based energy acceptor systems and sensors ». Journal of Photochemistry and Photobiology C : Photochemistry Reviews 18 (mars 2014) : 1–17. http://dx.doi.org/10.1016/j.jphotochemrev.2013.10.002.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

23

Kachkovskii, A. D., et N. M. Kovalenko. « Conformation transformation barriers in linear donor-acceptor systems ». Theoretical and Experimental Chemistry 33, n^o 4 (juillet 1997) : 192–95. http://dx.doi.org/10.1007/bf02764767.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

24

Kang, E. T. « Charge transfer interactions in polyphenylacetylene-electron acceptor systems ». European Polymer Journal 21, n^o 11 (janvier 1985) : 919–24. http://dx.doi.org/10.1016/0014-3057(85)90176-4.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

25

Merkli, Marco, Gennady P. Berman et Avadh Saxena. « Quantum electron transport in degenerate donor–acceptor systems ». Journal of Mathematical Physics 61, n^o 7 (1 juillet 2020) : 072102. http://dx.doi.org/10.1063/1.5138725.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

26

Hurenkamp, Johannes H., Jaap J. D. de Jong, Wesley R. Browne, Jan H. van Esch et Ben L. Feringa. « Tuning energy transfer in switchable donor–acceptor systems ». Organic & ; Biomolecular Chemistry 6, n^o 7 (2008) : 1268. http://dx.doi.org/10.1039/b719095f.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

27

Vijatović Petrović, M. M., J. D. Bobić, R. Grigalaitis, N. I. Ilic, A. S. Dzunuzovic, V. Jankauskaite, J. Banys et B. D. Stojanović. « Donor–acceptor joint effect in barium titanate systems ». Ceramics International 41, n^o 9 (novembre 2015) : 11365–71. http://dx.doi.org/10.1016/j.ceramint.2015.05.096.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

28

Blok, Victor R., et Gennady M. Krochik. « Photo-transfer of electrons in donor-acceptor systems ». Solid State Communications 75, n^o 1 (juillet 1990) : 11–15. http://dx.doi.org/10.1016/0038-1098(90)90148-5.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

29

Miro, Paula, Ignacio Vayá, Germán Sastre, M. Consuelo Jiménez, M. Luisa Marin et Miguel A. Miranda. « Triplet energy management between two signaling units through cooperative rigid scaffolds ». Chemical Communications 52, n^o 4 (2016) : 713–16. http://dx.doi.org/10.1039/c5cc08102e.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

30

Arrechea, Susana, Agustín Molina-Ontoria, Ana Aljarilla, Pilar de la Cruz, Fernando Langa et Luis Echegoyen. « New acceptor–π-porphyrin–π-acceptor systems for solution-processed small molecule organic solar cells ». Dyes and Pigments 121 (octobre 2015) : 109–17. http://dx.doi.org/10.1016/j.dyepig.2015.04.037.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

31

Salmerón-valverde, A., J. G. Robles-Martínez, J. García-serrano, R. Gómez, R. Ridaura, M. Quintana et A. Zehe. « Effects of Acceptor Modification on Charge Transfer in Crystals of Donor-Acceptor Systems of TTF ». Crystal Research and Technology 32, n^o 5 (1997) : 717–22. http://dx.doi.org/10.1002/crat.2170320516.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

32

Medyakova, L. V., Zakir M. O. Rzaev, Ali G�ner et G�nay Kibarer. « Complex-radical terpolymerization of acceptor-donor-acceptor systems : Maleic anhydride (n-butyl methacrylate)-styrene-acrylonitrile ». Journal of Polymer Science Part A : Polymer Chemistry 38, n^o 15 (2000) : 2652–62. http://dx.doi.org/10.1002/1099-0518(20000801)38:15<2652 ::aid-pola40>3.0.co;2-b.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

33

Ming, Shouli, Shijie Zhen, Ximei Liu, Kaiwen Lin, Hongtao Liu, Yao Zhao, Baoyang Lu et Jingkun Xu. « Chalcogenodiazolo[3,4-c]pyridine based donor–acceptor–donor polymers for green and near-infrared electrochromics ». Polymer Chemistry 6, n^o 48 (2015) : 8248–58. http://dx.doi.org/10.1039/c5py01321f.

Texte intégral

Résumé :

Thiadiazolo[3,4-c]pyridine and selenadiazolo[3,4-c]pyridine were employed as novel acceptors for rational design of donor-acceptor-type systems, yielding neutral green and near-infrared electrochromic polymers.

Styles APA, Harvard, Vancouver, ISO, etc.

34

Razus, Alexandru C. « Azulene Moiety as Electron Reservoir in Positively Charged Systems ; A Short Survey ». Symmetry 13, n^o 4 (24 mars 2021) : 526. http://dx.doi.org/10.3390/sym13040526.

Texte intégral

Résumé :

The non-alternant aromatic azulene, an isomer of alternant naphthalene, differs from the latter in peculiar properties. The large polarization of the π-electron system over the seven and five rings gives to azulene electrophile property a pronounced tendency to donate electrons to an acceptor, substituted at azulene 1 position. This paper presents cases in which azulene transfers electrons to a suitable acceptor as methylium ions, positive charged heteroaromatics and examples of neutral molecules that can accept electrons. The proposed product synthesis was outlined and the expected electron transfer was highlighted by analyzing the NMR, UV-Vis spectra and the pKR+ values.

Styles APA, Harvard, Vancouver, ISO, etc.

35

D'Souza, Francis, et V. Krishnan. « INTRAMOLECULAR DONOR-ACCEPTOR SYSTEMS : STRUCTURES OF NOVEL LINKED PORPHYRIN- PHENOLPHTHALEIN MOLECULAR SYSTEMS ». Photochemistry and Photobiology 51, n^o 3 (mars 1990) : 285–91. http://dx.doi.org/10.1111/j.1751-1097.1990.tb01712.x.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

36

Das, Paramita, Ray J. Butcher et Chhanda Mukhopadhyay. « Zinc titanate nanopowder : an advanced nanotechnology based recyclable heterogeneous catalyst for the one-pot selective synthesis of self-aggregated low-molecular mass acceptor–donor–acceptor–acceptor systems and acceptor–donor–acceptor triads ». Green Chemistry 14, n^o 5 (2012) : 1376. http://dx.doi.org/10.1039/c2gc16641k.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

37

Wei, Zimu, Sushil Sharma, Abbey M. Philip, Sanchita Sengupta et Ferdinand C. Grozema. « Excited state dynamics of BODIPY-based acceptor–donor–acceptor systems : a combined experimental and computational study ». Physical Chemistry Chemical Physics 23, n^o 14 (2021) : 8900–8907. http://dx.doi.org/10.1039/d1cp00453k.

Texte intégral

Résumé :

Donor-bridge-acceptor systems based on boron dipyrromethene (BODIPY) are attractive candidates for bio-imagining and sensing applications because of their sensitivity to temperature, micro-viscosity and solvent polarity.

Styles APA, Harvard, Vancouver, ISO, etc.

38

Shun-Lai, Li, Dong Xiao-Yang et Xu Hui-Jun. « Intramolecular Photoinduced Electron Transfer in Donor-BA-Acceptor Systems ». Acta Physico-Chimica Sinica 13, n^o 08 (1997) : 680–84. http://dx.doi.org/10.3866/pku.whxb19970802.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

39

SHIROTA, Yasuhiko, Kentaro YAMAGUCHI, Shin-Chol OH, Satoshi MASUMI et Guang-Jie JIANG. « PHOTOPOLYMERIZATIONS OF ELECTRON-DONOR MONOMER-ELECTRON-ACCEPTOR MONOMER SYSTEMS ». Journal of Photopolymer Science and Technology 1, n^o 2 (1988) : 346–53. http://dx.doi.org/10.2494/photopolymer.1.346.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

40

Colquhoun, Howard M., Barnaby W. Greenland, Zhixue Zhu, John S. Shaw, Christine J. Cardin, Stefano Burattini, Joanne M. Elliott, Subhadeep Basu, Travis B. Gasa et J. Fraser Stoddart. « A General Synthesis of Macrocyclic π-Electron-Acceptor Systems ». Organic Letters 11, n^o 22 (19 novembre 2009) : 5238–41. http://dx.doi.org/10.1021/ol9021782.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

41

Shizu, Katsuyuki, Jiyoung Lee, Hiroyuki Tanaka, Hiroko Nomura, Takuma Yasuda, Hironori Kaji et Chihaya Adachi. « Highly efficient electroluminescence from purely organic donor–acceptor systems ». Pure and Applied Chemistry 87, n^o 7 (1 juillet 2015) : 627–38. http://dx.doi.org/10.1515/pac-2015-0301.

Texte intégral

Résumé :

AbstractThermally activated delayed fluorescence (TADF) emitters are third-generation electroluminescent materials that realize highly efficient organic light-emitting diodes (OLEDs) without using rare metals. Here, after briefly reviewing the principles of TADF and its use in OLEDs, we report a sky-blue TADF emitter, 9-(4-(benzo[d]thiazol-2-yl)phenyl)-N3,N3,N6,N6-tetraphenyl-9H-carbazole-3,6-diamine (DAC-BTZ). DAC-BTZ is a purely organic donor–acceptor-type molecule with a small energy difference between its lowest excited singlet state and lowest triplet state of 0.18–0.22 eV according to fluorescence and phosphorescence spectra of a DAC-BTZ-doped film. In addition, the doped film exhibits a high photoluminescence quantum yield of 0.82. Time-resolved photoluminescence measurements of the doped film confirm that DAC-BTZ emits TADF. An OLED containing DAC-BTZ as an emitter exhibits a maximum external quantum efficiency (EQE) of 10.3%, which exceeds those obtained with conventional fluorescent emitters (5–7.5%). TADF from DAC-BTZ makes a large contribution to the high EQE of its OLED.

Styles APA, Harvard, Vancouver, ISO, etc.

42

Vannikov, Anatolii V., et Antonina D. Grishina. « Spectral Sensitisation of Photoprocesses in Polymeric Donor–Acceptor Systems ». Russian Chemical Reviews 56, n^o 7 (31 juillet 1987) : 633–52. http://dx.doi.org/10.1070/rc1987v056n07abeh003295.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

43

Yagupolskii, Lev M., Vitalij N. Petrik et Yurij L. Slominskii. « N-Trifluoromethylsulfonylimino derivatives of carbonyl-containing donor–acceptor systems ». Tetrahedron Letters 43, n^o 21 (mai 2002) : 3957–59. http://dx.doi.org/10.1016/s0040-4039(02)00586-5.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

44

Dissanayake, Dhammike P., et M. D. P. De Costa. « Fluorescence Characteristics of [(Benzoyloxy)methyl]anthracene Donor–Acceptor Systems ». Journal of Physical Chemistry A 119, n^o 29 (30 juin 2015) : 7973–79. http://dx.doi.org/10.1021/acs.jpca.5b01451.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

45

Cooray, Anusha S., et K. M. Nalin de Silva. « Theoretical investigations of self-organising donor–acceptor aromatic systems ». Journal of Molecular Structure : THEOCHEM 678, n^o 1-3 (juin 2004) : 223–31. http://dx.doi.org/10.1016/j.theochem.2004.02.048.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

46

Imahori, Hiroshi. « (Invited) Photoinduced Donor-Acceptor Interaction in Nanocarbon-Based Systems ». ECS Meeting Abstracts MA2020-01, n^o 9 (1 mai 2020) : 802. http://dx.doi.org/10.1149/ma2020-019802mtgabs.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

47

Drigo, Nikita A., Sanghyun Paek, Aron J. Huckaba, Pascal A. Schouwink, Nouar Tabet et Mohammad K. Nazeeruddin. « Approaches for Selective Synthesis of Ullazine Donor-Acceptor Systems ». Chemistry - A European Journal 23, n^o 68 (20 novembre 2017) : 17209–12. http://dx.doi.org/10.1002/chem.201704694.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

48

Coutinho-Neto, Maurício D., et A. Arnóbio de S. da Gama. « Donor-acceptor interaction in two-level-reduced molecular systems ». Chemical Physics 203, n^o 1 (février 1996) : 43–52. http://dx.doi.org/10.1016/0301-0104(95)00320-7.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

49

Heitele, H., M. E. Michel-Beyerle et P. Finckh. « Electron transfer through intramolecular bridges in donor/acceptor systems ». Chemical Physics Letters 134, n^o 3 (février 1987) : 273–78. http://dx.doi.org/10.1016/0009-2614(87)87135-x.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

50

Psiachos, D. « Short-lived electron transfer in donor-bridge-acceptor systems ». Chemical Physics Letters 662 (octobre 2016) : 201–7. http://dx.doi.org/10.1016/j.cplett.2016.09.034.

Texte intégral

Styles APA, Harvard, Vancouver, ISO, etc.

Articles de revues sur le sujet « Acceptor Systems »

Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres