Bibliografías temáticas / Conjugated and cumulated molecules / Artículos de revistas

Artículos de revistas sobre el tema "Conjugated and cumulated molecules"

Siga este enlace para ver otros tipos de publicaciones sobre el tema: Conjugated and cumulated molecules.
Autor: Grafiati
Publicado: 18 de mayo de 2024

Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros

Elija tipo de fuente:

Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Conjugated and cumulated molecules".

Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.

También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.

Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.

1

Sarbadhikary, Prodipta, Suranjan Shil y Anirban Misra. "Magnetic and transport properties of conjugated and cumulated molecules: the π-system enlightens part of the story". Physical Chemistry Chemical Physics 20, n.º 14 (2018): 9364–75. http://dx.doi.org/10.1039/c7cp06113g.

Texto completo
Resumen
We have investigated the intramolecular magnetic exchange coupling constants (J) for a series of nitronyl nitroxide diradicals connected by a range of linear conjugated and cumulene couplers focusing on the unusual π-interaction properties within the couplers.
Los estilos APA, Harvard, Vancouver, ISO, etc.
2

Horká, Petra, Vladimír Vrkoslav, Jiří Kindl, Karolina Schwarzová-Pecková y Josef Cvačka. "Structural Characterization of Unusual Fatty Acid Methyl Esters with Double and Triple Bonds Using HPLC/APCI-MS2 with Acetonitrile In-Source Derivatization". Molecules 26, n.º 21 (26 de octubre de 2021): 6468. http://dx.doi.org/10.3390/molecules26216468.

Texto completo
Resumen
Double and triple bonds have significant effects on the biological activities of lipids. Determining multiple bond positions in their molecules by mass spectrometry usually requires chemical derivatization. This work presents an HPLC/MS method for pinpointing the double and triple bonds in fatty acids. Fatty acid methyl esters were separated by reversed-phase HPLC with an acetonitrile mobile phase. In the APCI source, acetonitrile formed reactive species, which added to double and triple bonds to form [M + C3H5N]+• ions. Their collisional activation in an ion trap provided fragments helpful in localizing the multiple bond positions. This approach was applied to fatty acids with isolated, cumulated, and conjugated double bonds and triple bonds. The fatty acids were isolated from the fat body of early-nesting bumblebee Bombus pratorum and seeds or seed oils of Punicum granatum, Marrubium vulgare, and Santalum album. Using the method, the presence of the known fatty acids was confirmed, and new ones were discovered.
Los estilos APA, Harvard, Vancouver, ISO, etc.
3

Renard, Emma, Olivier Raguin, Victor Goncalves, Celine Mothes, Mathieu Moreau, Claire Bernhard, Peggy Provent et al. "Abstract 1401: Lead optimization of radiopharmaceuticals for molecular radiotherapy and preclinical evaluation". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 1401. http://dx.doi.org/10.1158/1538-7445.am2022-1401.

Texto completo
Resumen
Abstract Molecular Radiotherapy (MRT) targeting SSTR2 or PSMA have proven to be highly efficient for the treatment of neuroendocrine or metastatic prostate cancer, respectively. Beyond the leading radiopharmaceutical molecules 177Lu-DOTATATE or 177Lu-PSMA-617, a variety of vectors (small molecules, peptides, panel of biologics) have been developed on the same targets in order to improve the biodistribution within the tumor, the blood clearance, the route of elimination or the dosimetry. The labeling of the targeting ligand, whatever its nature, is a crucial step as it may affect significantly the properties of the theranostic conjugate, i.e. its binding affinity, PK and biodistribution. The addition of linkers, such as albumin binding domain or PEG, and choice of chelating agents have a major impact on the chemical and biological properties of the vectors. Random or site-specific bioconjugation, click chemistry, also have to be considered in the early stage as the choice of the selected technology will modify your development plan and manufacturing. New ligands and biological platforms are now being developed based on this historical knowledge, improved Target Product Profiles are built to conduct optimal lead optimization of MRT. Herein, we will present our lead optimization and preclinical evaluation process to select efficiently good radiolabeled molecules and list the key parameters to be checked. To date, it remains hard to predict the behavior of the modified bioconjugated molecules, and versatile synthesis strategies are needed to screen various combinations of radiometal complexes, linker and conjugation function, in order to converge rapidly to the optimized bioconjugate. As an example, we will present a study case where the conjugation of various bifunctional chelating agents on a small NTS1 receptor antagonist resulted in drastically different in vivo behavior of the resulting 68Ga-labeled compounds. Once optimal in vivo tumor uptake has been achieved, preclinical evaluation requires the selection of appropriate and relevant models, driven by target expression, radioresistance, and potentially tumor immune infiltrate for combination studies with immunotherapies. The therapeutic evaluation should take into consideration the dose and specific activity, the tolerance of a model related to ionizing radiations and the scheduling of treatments (cumulated dose, fractionation). We will present our recent results which highlight the importance to optimize these parameters to improve the efficacy of MRT. Citation Format: Emma Renard, Olivier Raguin, Victor Goncalves, Celine Mothes, Mathieu Moreau, Claire Bernhard, Peggy Provent, Frederic Boschetti, Franck Denat, Fabrice Viviani, Cyril Berthet. Lead optimization of radiopharmaceuticals for molecular radiotherapy and preclinical evaluation [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2022; 2022 Apr 8-13. Philadelphia (PA): AACR; Cancer Res 2022;82(12_Suppl):Abstract nr 1401.
Los estilos APA, Harvard, Vancouver, ISO, etc.
4

van Dongen, J. P. C. M., A. J. de Jong, H. A. Selling, P. P. Montijn, J. H. van Boom y L. Brandsma. "Isomerization of conjugated and cumulated systems". Recueil des Travaux Chimiques des Pays-Bas 86, n.º 10 (2 de septiembre de 2010): 1077–81. http://dx.doi.org/10.1002/recl.19670861008.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
5

Schonk, Ruud M., Bert H. Bakker y Hans Cerfontain. "Reactions of cumulated and conjugated dienes with sulfur trioxide". Recueil des Travaux Chimiques des Pays-Bas 112, n.º 3 (2 de septiembre de 2010): 201–9. http://dx.doi.org/10.1002/recl.19931120301.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
6

Zhu, Xiao-Qing, Hao Liang, Yan Zhu y Jin-Pei Cheng. "Hydride Affinities of Cumulated, Isolated, and Conjugated Dienes in Acetonitrile". Journal of Organic Chemistry 73, n.º 21 (7 de noviembre de 2008): 8403–10. http://dx.doi.org/10.1021/jo801536m.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
7

H. Muhammad, G. Tastemirova y K. Abdibekova. "STRUCTURES OF ALKANDIENES IN HYDROCARBONS". Bulletin of Toraighyrov University. Chemistry & Biology series, n.º 4.2022 (28 de diciembre de 2022): 19–33. http://dx.doi.org/10.48081/rglj8585.

Texto completo
Resumen
"Alkadienes have been under study for a long time, until the last decade of the 19th century, various structures have been known, each structure represents the specific chemical properties of the compound, alkadienes structures are the first important step for better identification of these compounds, by identifying the structures, different types of alkadienes can be distinguished from each other. Also, the structures of alkadienes and important synthetic compounds are of great value in industry and medicine. Conjugated, isolated, and cumulated structures have been identified by different people at different times in alkadienes. Compounds of alkadienes i.e. conjugated, isolated and cumulated alkadienes have chain and cyclic structures, alkadienes are used as medicine to treat some deadly diseases, for example Taxol in 1960, Jonathan Hartwell in the United States collected some plants such as pacific yew for the treatment of breast cancer. Also, in the 19th century, synthetic and natural polymers of alkadienes were widely used in the tire industry, in general, alkadienes are compounds that have two carbon-carbon double bonds (π) in their composition, that is why they are very active compounds, it is widely used in industry all over the world and they have caused the development of the world’s economy and industry. Keywords: Alkadienes, Nomenclature of alkadienes, Conjugated alkadienes, stability of conjugated alkadienes, Ultraviolet spectroscopy. "
Los estilos APA, Harvard, Vancouver, ISO, etc.
8

Nuckolls, Colin, Thomas J. Katz y Louis Castellanos. "Aggregation of Conjugated Helical Molecules". Journal of the American Chemical Society 118, n.º 15 (enero de 1996): 3767–68. http://dx.doi.org/10.1021/ja960145z.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
9

Dias, Jerry Ray. "Almost-isospectral conjugated polyene molecules". Chemical Physics Letters 253, n.º 3-4 (mayo de 1996): 305–12. http://dx.doi.org/10.1016/0009-2614(96)00258-8.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
10

Fox, J., Z. Dong, X. Liu y G. Yap. "Parallel Alignment of Conjugated Rod Molecules". Synfacts 2007, n.º 4 (abril de 2007): 0384. http://dx.doi.org/10.1055/s-2007-968319.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
11

Weber, H. B., J. Reichert, F. Weigend, R. Ochs, D. Beckmann, M. Mayor, R. Ahlrichs y H. v. Löhneysen. "Electronic transport through single conjugated molecules". Chemical Physics 281, n.º 2-3 (agosto de 2002): 113–25. http://dx.doi.org/10.1016/s0301-0104(02)00343-9.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
12

Burn, P. L., R. Beavington, M. J. Frampton, J. N. G. Pillow, M. Halim, J. M. Lupton y I. D. W. Samuel. "Structure–property relationships in conjugated molecules". Materials Science and Engineering: B 85, n.º 2-3 (agosto de 2001): 190–94. http://dx.doi.org/10.1016/s0921-5107(01)00609-2.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
13

Almeida, A. M., M. M. D. Ramos y H. G. Correia. "Change mobility in conjugated polymer molecules". Computational Materials Science 27, n.º 1-2 (marzo de 2003): 128–32. http://dx.doi.org/10.1016/s0927-0256(02)00436-6.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
14

SCHONK, R. M., B. H. BAKKER y H. CERFONTAIN. "ChemInform Abstract: Aliphatic Sulfonation. Part 11. Reactions of Cumulated and Conjugated Dienes with Sulfur Trioxide." ChemInform 24, n.º 32 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199332108.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
15

Yang, Chunhe, Aiwei Tang, Fujun Zhang y Feng Teng. "DFT investigation on organic dyes with cross-conjugated cyano groups". Journal of Theoretical and Computational Chemistry 13, n.º 01 (febrero de 2014): 1450008. http://dx.doi.org/10.1142/s0219633614500084.

Texto completo
Resumen
Organic dye molecules with the acceptor moieties, cyano groups, cross-conjugated to the donor moieties, have been investigated theoretically. Density functional theory (DFT) calculations on such cross-conjugated molecules reveal the effects of cross-conjugation on the geometric and electronic structures of the molecules. The cross-conjugated cyano groups in the dye molecules are found effective to alter the charge population and the frontier orbital energy levels of the dyes. The effects of cross-conjugation of cyano group on the molecular conformation, the charge transfer, and polarity of the dyes are discussed.
Los estilos APA, Harvard, Vancouver, ISO, etc.
16

Maeda, Hiromitsu y Yuya Bando. "Recent progress in research on stimuli-responsive circularly polarized luminescence based on π-conjugated molecules". Pure and Applied Chemistry 85, n.º 10 (1 de octubre de 2013): 1967–78. http://dx.doi.org/10.1351/pac-con-12-11-09.

Texto completo
Resumen
This short review article summarizes recent progress in research on various stimuli-responsive circularly polarized luminescence (CPL) properties derived from π-conjugated molecules and related materials. As representative examples, assembled structures of chiral π-conjugated polymers and molecules showed tunable CPL resulting from the enhancement of chirality induction by aggregation. Fascinating CPL-active species, pyrrole-based anion-responsive π-conjugated molecules exhibiting CPL induced by anion binding and ion pairing, are also discussed.
Los estilos APA, Harvard, Vancouver, ISO, etc.
17

Ogata, Makoto. "Functional design of glycan-conjugated molecules using a chemoenzymatic approach". Bioscience, Biotechnology, and Biochemistry 85, n.º 5 (15 de febrero de 2021): 1046–55. http://dx.doi.org/10.1093/bbb/zbab024.

Texto completo
Resumen
ABSTRACT Carbohydrates play important and diverse roles in the fundamental processes of life. We have established a method for accurately and a large-scale synthesis of functional carbohydrates with diverse properties using a unique enzymatic method. Furthermore, various artificial glycan-conjugated molecules have been developed by adding these synthetic carbohydrates to macromolecules and to middle- and low-molecular-weight molecules with different properties. These glycan-conjugated molecules have biological activities comparable to or higher than those of natural compounds and present unique functions. In this review, several synthetic glycan-conjugated molecules are taken as examples to show design, synthesis, and function.
Los estilos APA, Harvard, Vancouver, ISO, etc.
18

Orita, Akihiro, Lasheng Jiang, Madoka Tsuruta y Junzo Otera. "Novel π-Conjugated Cyclophanes: Magazine Rack Molecules". Chemistry Letters 31, n.º 2 (febrero de 2002): 136–37. http://dx.doi.org/10.1246/cl.2002.136.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
19

Aoki, Yuriko, Yuuichi Orimoto y Akira Imamura. "One-Handed Helical Orbitals in Conjugated Molecules". ACS Central Science 4, n.º 6 (16 de mayo de 2018): 664–65. http://dx.doi.org/10.1021/acscentsci.8b00228.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
20

Aihara, Jun-ichi, Hideaki Kanno y Toshimasa Ishida. "Magnetic Resonance Energies of Heterocyclic Conjugated Molecules". Journal of Physical Chemistry A 111, n.º 36 (septiembre de 2007): 8873–76. http://dx.doi.org/10.1021/jp0733567.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
21

Zhang, Fuji y Huaien Li. "On acyclic conjugated molecules with minimal energies". Discrete Applied Mathematics 92, n.º 1 (marzo de 1999): 71–84. http://dx.doi.org/10.1016/s0166-218x(98)00152-8.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
22

Bjorgaard, Josiah A., Andrew E. Sifain, Tammie Nelson, Thomas W. Myers, Jacqueline M. Veauthier, David E. Chavez, R. Jason Scharff y Sergei Tretiak. "Two-Photon Absorption in Conjugated Energetic Molecules". Journal of Physical Chemistry A 120, n.º 26 (23 de junio de 2016): 4455–64. http://dx.doi.org/10.1021/acs.jpca.6b03136.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
23

Li, Xueliang, Jianbin Zhang y Bo Zhou. "On unicyclic conjugated molecules with minimal energies". Journal of Mathematical Chemistry 42, n.º 4 (10 de octubre de 2006): 729–40. http://dx.doi.org/10.1007/s10910-006-9116-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
24

Gierschner, J., H. J. Egelhaaf, H. G. Mack, D. Oelkrug, R. Martinez Alvarez y M. Hanack. "Luminescence of Conjugated Molecules Confined in Nanochannels". Synthetic Metals 137, n.º 1-3 (abril de 2003): 1449–50. http://dx.doi.org/10.1016/s0379-6779(02)01175-x.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
25

Yamamoto, Yohei. "Electroactive Nanotubes from π-Conjugated Discotic Molecules". Bulletin of the Chemical Society of Japan 84, n.º 1 (15 de enero de 2011): 17–25. http://dx.doi.org/10.1246/bcsj.20100272.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
26

Vasil’eva, I. A. "Fine-Structure Fluorescence of Conjugated Chain Molecules". Optics and Spectroscopy 98, n.º 5 (2005): 753. http://dx.doi.org/10.1134/1.1929062.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
27

Hendon, Christopher H., Davide Tiana, Alexander T. Murray, David R. Carbery y Aron Walsh. "Helical frontier orbitals of conjugated linear molecules". Chemical Science 4, n.º 11 (2013): 4278. http://dx.doi.org/10.1039/c3sc52061g.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
28

Meimel, Georg, Alexander Pogantsch y Egbert Zojer. "Exciton-Phonon Coupling in Conjugated Organic Molecules". Physica Scripta T109 (2004): 156. http://dx.doi.org/10.1238/physica.topical.109a00156.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
29

Terao, Jun. "π-conjugated molecules covered by permethylated cyclodextrins". Chemical Record 11, n.º 5 (7 de septiembre de 2011): 269–83. http://dx.doi.org/10.1002/tcr.201100009.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
30

Samorí, Paolo, Xinliang Feng y Davide Bonifazi. "π‐Conjugated Molecules: From Structure to Function". ChemPlusChem 84, n.º 9 (23 de agosto de 2019): 1177–78. http://dx.doi.org/10.1002/cplu.201900442.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
31

Dumonteil, Geoffrey y Sabine Berteina-Raboin. "Synthesis of Conjugated Dienes in Natural Compounds". Catalysts 12, n.º 1 (13 de enero de 2022): 86. http://dx.doi.org/10.3390/catal12010086.

Texto completo
Resumen
This review describes the various synthetic methods commonly used to obtain molecules possessing conjugated dienes. We focus on methods involving cross-coupling reactions using various metals such as nickel, palladium, ruthenium, cobalt, cobalt/zinc, manganese, zirconium, or iron, mainly through examples that aimed to access natural molecules or their analogues. Among the natural molecules covered in this review, we discuss the total synthesis of a phytohormone, Acid Abscisic (ABA), carried out by our team involving the development of a conjugated diene chain.
Los estilos APA, Harvard, Vancouver, ISO, etc.
32

An, Cunbin, Yunpeng Qin, Tao Zhang, Qianglong Lv, Jinzhao Qin, Shaoqing Zhang, Chang He, Harald Ade y Jianhui Hou. "Optimization of active layer morphology by small-molecule donor design enables over 15% efficiency in small-molecule organic solar cells". Journal of Materials Chemistry A 9, n.º 23 (2021): 13653–60. http://dx.doi.org/10.1039/d0ta12242d.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
33

Hiroto, Satoru. "Development of synthetic protocols for porphyrins and their analogs based on distorted structures — a SPP/JPP Young Investigator Award paper". Journal of Porphyrins and Phthalocyanines 24, n.º 11n12 (21 de octubre de 2020): 1258–71. http://dx.doi.org/10.1142/s1088424620500376.

Texto completo
Resumen
Creation of novel [Formula: see text]-conjugated molecules is an important research topic. I describe in this account an approach to this aim that is based on the use of the distorted conformation of porphyrins. Planarization of distorted molecules enables the synthesis of heteroatom-containing porphyrin derivatives. Furthermore, dearomatization reaction proves effective to construct distorted conformations from planar [Formula: see text]-conjugated molecules under mild reaction conditions. According to this protocol, we have succeeded in the synthesis of heteroatom-containing curved-[Formula: see text] conjugated molecules that had never been achieved by conventional protocols. In particular, a nitrogen-embedded buckybowl is the first example of a buckybowl having a heteroatom in its central position, which exhibits unique properties due to the incorporation of the heteroatom in its curved [Formula: see text]-surface.
Los estilos APA, Harvard, Vancouver, ISO, etc.
34

Randić, Milan, Sonja Nikolić y Nenad Trinajstić. "Aromaticity in heterocyclic molecules containing divalent sulfur". Collection of Czechoslovak Chemical Communications 53, n.º 9 (1988): 2023–54. http://dx.doi.org/10.1135/cccc19882023.

Texto completo
Resumen
The conjugated circuits model is applied to heterocycles containing divalent sulfur. A novel parametrization is introduced for 4n + 2 and 4n conjugated circuits containing a single sulfur atom. The relative aromatic stabilities of a number of heterocyclic systems containing divalent sulfur are studied. Comparison is made whenever possible with earlier reported resonance energies of these compounds, obtained by using Huckel MO and SCF π-MO models, and appropriate reference structures. Special attention is given to positional isomers. An explanation of the differences amongst such isomers is given.
Los estilos APA, Harvard, Vancouver, ISO, etc.
35

Hiroto, Satoru y Hiroshi Shinokubo. "Synthesis of Heteroatom-Containing Curved π-Conjugated Molecules". Journal of Synthetic Organic Chemistry, Japan 76, n.º 1 (2018): 37–44. http://dx.doi.org/10.5059/yukigoseikyokaishi.76.37.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
36

Ha Hoang, Mai, Duc Nghia Nguyen y Dong Hoon Choi. "π-extended conjugated semiconducting molecules based on triphenylene". Advances in Natural Sciences: Nanoscience and Nanotechnology 2, n.º 3 (21 de junio de 2011): 035002. http://dx.doi.org/10.1088/2043-6262/2/3/035002.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
37

Dadosh, Tali, Yoav Gordin, Roman Krahne, Ilya Khivrich, Diana Mahalu, Veronica Frydman, Joseph Sperling, Amir Yacoby y Israel Bar-Joseph. "Measurement of the conductance of single conjugated molecules". Nature 436, n.º 7051 (4 de agosto de 2005): 677–80. http://dx.doi.org/10.1038/nature03898.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
38

Matsushita, Michio M., Tomoyuki Tachikawa, Takehiko Suzuki, Tadashi Kawai y Tomokazu Iyoda. "Photoelectrochemical Spin Manipulation of N-Arylviologen Conjugated Molecules". Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 334, n.º 1 (1 de septiembre de 1999): 149–56. http://dx.doi.org/10.1080/10587259908023312.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
39

Liang, Y. Y., Y. X. Zhou, H. Chen, R. Note, H. Mizuseki y Y. Kawazoe. "Current through single conjugated molecules: Calculations versus measurements". Journal of Chemical Physics 129, n.º 2 (14 de julio de 2008): 024901. http://dx.doi.org/10.1063/1.2951986.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
40

Gel’mukhanov, Faris, Li Yang y Hans Ågren. "Theory of x‐ray emission of conjugated molecules". Journal of Chemical Physics 105, n.º 12 (22 de septiembre de 1996): 5224–32. http://dx.doi.org/10.1063/1.472365.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
41

Lu, Mei, Lian-zhu Zhang y Feng Tian. "On the Randić Index of Acyclic Conjugated Molecules". Journal of Mathematical Chemistry 38, n.º 4 (noviembre de 2005): 677–84. http://dx.doi.org/10.1007/s10910-005-6892-4.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
42

Liu, Huiqing, Xiangfeng Pan y Jun-Ming Xu. "On the Randić Index of Unicyclic Conjugated Molecules". Journal of Mathematical Chemistry 40, n.º 2 (13 de marzo de 2006): 135–43. http://dx.doi.org/10.1007/s10910-005-9017-1.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
43

Mizoguchi, Noriyuki. "H�ckel and M�bius cyclic conjugated molecules". Journal of Mathematical Chemistry 7, n.º 1 (diciembre de 1991): 325–40. http://dx.doi.org/10.1007/bf01200830.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
44

Sixl, H. y R. Warta. "Elementary excitations in linear-chain conjugated polydiacetylene molecules". Chemical Physics Letters 116, n.º 4 (mayo de 1985): 307–11. http://dx.doi.org/10.1016/0009-2614(85)80174-3.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
45

Li, Xiaolong, Hongmei Liu y Jianwei Zhao. "Length-dependent Conductance in Conjugated Molecules in Parallel". Chemistry Letters 44, n.º 2 (5 de febrero de 2015): 208–10. http://dx.doi.org/10.1246/cl.140969.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
46

Lovey, D. A. y R. H. Romero. "CONDUCTANCE AND ELECTRONIC STRUCTURE OF CONJUGATED ORGANIC MOLECULES". Anales AFA 23, n.º 1 (29 de julio de 2013): 171–75. http://dx.doi.org/10.31527/analesafa.2013.23.1.171.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
47

Ohmae, Takayuki. "Solvent Effects on Chemical Reactivities of Conjugated Molecules". Bulletin of the Chemical Society of Japan 58, n.º 1 (enero de 1985): 47–51. http://dx.doi.org/10.1246/bcsj.58.47.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
48

Maeda, Hiromitsu. "Supramolecular Chemistry of Pyrrole-Based π-Conjugated Molecules". Bulletin of the Chemical Society of Japan 86, n.º 12 (15 de diciembre de 2013): 1359–99. http://dx.doi.org/10.1246/bcsj.20130219.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
49

Tretiak, S., A. Saxena, R. L. Martin y A. R. Bishop. "Geometry Relaxation of Photoexcited States in Conjugated Molecules". Phase Transitions 75, n.º 7-8 (enero de 2002): 725–32. http://dx.doi.org/10.1080/01411590290033831.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
50

Ferrante, C., A. Speghini, A. Feis y R. Bozio. "Resonance CARS of conjugated molecules in condensed phase". Il Nuovo Cimento D 14, n.º 10 (octubre de 1992): 1015–22. http://dx.doi.org/10.1007/bf02455363.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
También puede estar interesado en las bibliografías sobre el tema "Conjugated and cumulated molecules" para otros tipos de fuentes:
Tesis
Ofrecemos descuentos en todos los planes premium para autores cuyas obras están incluidas en selecciones literarias temáticas. ¡Contáctenos para obtener un código promocional único!

Pasar a la bibliografía