Letteratura scientifica selezionata sul tema "Complexes bioinspirés"
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Articoli di riviste sul tema "Complexes bioinspirés":
Chaignon, Jérémy, Marie Gourgues, Lhoussain Khrouz, Nicolás Moliner, Laurent Bonneviot, Fabienne Fache, Isabel Castro e Belén Albela. "A bioinspired heterogeneous catalyst based on the model of the manganese-dependent dioxygenase for selective oxidation using dioxygen". RSC Advances 7, n. 28 (2017): 17336–45. http://dx.doi.org/10.1039/c7ra00514h.
Wu, Hao-Lin, Xu-Bing Li, Chen-Ho Tung e Li-Zhu Wu. "Bioinspired metal complexes for energy-related photocatalytic small molecule transformation". Chemical Communications 56, n. 99 (2020): 15496–512. http://dx.doi.org/10.1039/d0cc05870j.
Carrión, Erik N., Andrei Loas, Hemantbhai H. Patel, Marius Pelmuş, Karpagavalli Ramji e Sergiu M. Gorun. "Fluoroalkyl phthalocyanines: Bioinspired catalytic materials". Journal of Porphyrins and Phthalocyanines 22, n. 05 (17 aprile 2018): 371–97. http://dx.doi.org/10.1142/s1088424618500189.
Cook, Emma N., e Charles W. Machan. "Bioinspired mononuclear Mn complexes for O2 activation and biologically relevant reactions". Dalton Transactions 50, n. 46 (2021): 16871–86. http://dx.doi.org/10.1039/d1dt03178c.
Kung, Mayfair C., Mark V. Riofski, Michael N. Missaghi e Harold H. Kung. "Organosilicon platforms: bridging homogeneous, heterogeneous, and bioinspired catalysis". Chem. Commun. 50, n. 25 (2014): 3262–76. http://dx.doi.org/10.1039/c3cc48766k.
Zheng, Z., X. Huang, M. Schenderlein, H. Moehwald, G. K. Xu e D. G. Shchukin. "Bioinspired nanovalves with selective permeability and pH sensitivity". Nanoscale 7, n. 6 (2015): 2409–16. http://dx.doi.org/10.1039/c4nr06378c.
Mu, Ge, Ryan B. Gaynor, Baylee N. McIntyre, Bruno Donnadieu e Sidney E. Creutz. "Synthesis and Characterization of Bipyridyl-(Imidazole)n Mn(II) Compounds and Their Evaluation as Potential Precatalysts for Water Oxidation". Molecules 28, n. 20 (23 ottobre 2023): 7221. http://dx.doi.org/10.3390/molecules28207221.
Ehweiner, Madeleine A., Carina Vidovič, Ferdinand Belaj e Nadia C. Mösch-Zanetti. "Bioinspired Tungsten Complexes Employing a Thioether Scorpionate Ligand". Inorganic Chemistry 58, n. 12 (29 maggio 2019): 8179–87. http://dx.doi.org/10.1021/acs.inorgchem.9b00973.
Prat, Jacob R., Carlo A. Gaggioli, Ryan C. Cammarota, Eckhard Bill, Laura Gagliardi e Connie C. Lu. "Bioinspired Nickel Complexes Supported by an Iron Metalloligand". Inorganic Chemistry 59, n. 19 (21 settembre 2020): 14251–62. http://dx.doi.org/10.1021/acs.inorgchem.0c02041.
Sugimoto, Hideki, e Shinobu Itoh. "Oxidative Transformation of Alkenes Catalyzed by Bioinspired Osmium Complexes". Journal of Synthetic Organic Chemistry, Japan 75, n. 9 (2017): 929–40. http://dx.doi.org/10.5059/yukigoseikyokaishi.75.929.
Tesi sul tema "Complexes bioinspirés":
Beaume, Laëtitia. "Synthèse et étude de complexes di- et tri- nucléaires du fer inspirés du site actif des hydrogénases [FeFe]". Thesis, Brest, 2015. http://www.theses.fr/2015BRES0010/document.
Hydrogenases are metalloenzymes found in Nature which are able to catalyse the production and the uptake of dihydrogen. Reports orr the structures of these hydrogénases have revealed the organometallic nature of their active sites, which are based on bimetallic assemblies containing nickel and iron atoms. Therefore, many diiron complexes have been synthesized in order to understand and to reproduce the high efficiency of [FeFe]- hydrogenases towards the reversible conversion of protons into dihydrogen. In particular, dithiolato-bridged diiron compounds, with bidentate ligands, have been developed in reason of results of theoretical studies which have suggested that an asymmetrical disubstitution at one iron atom of such bioinspired molecules may allow to reproduce some structural key features of the active site. One part of the works reported in this thesis concems pursuing studies previously undertaken in the laboratory on the use of bidentate chelating ligands with diiron bioinspired models of [FeFe] hydrogenases, such as 1,10- phenanthroline or diphosphines. Another part reports the development of a systematîc way for the synthesis of original trinuclear iron clusters having a quasi-linear arrangement of the three iron atoms. Electrochemical behaviours of the synthesized species as well as their reactivity in acidic medium have been studied
Ségaud, Nathalie. "Étude de l’activation réductrice du dioxygène par un complexe de fer (II) et nouveaux complexes hétérodinucléaires : contributions pour le développement de catalyseurs d’oxydation bioinspirés". Thesis, Paris 11, 2013. http://www.theses.fr/2013PA112329/document.
MonoOxygenases (MO) such as cytochromes P450 catalyse the oxygen atom insertion into a chemical bond of an inert organic substrate following reductive activation of dioxygen. By using very simple Fe(II) complexes bearing amine/pyridine ligands, it is possible to prepare reactive species such as Fe(III)OOH and Fe(IV)O by using chemical oxidants (H2O2, peroxides, peracides...), or O2 in the presence of a chemical reductant via a reaction sequence similar to the one of P450. These intermediates have shown an efficient activity on hydroxylation of aromatic, and oxydation of olefins and alkanes. Nevertheless, these reactions suffer from a lack of specificity and regioselectivity. A drawback to the use of these complexes in oxidation catalysis by O2 is the side reaction between the oxidative intermediate species and the chemical reductant used. To solve these problems, different approaches have been developed during this thesis, in view to better mimic enzymes activity, and reproduce oxidation reactions efficiency and selectivity.A first strategy is to add an artificial cavity (calix[6]aren) to our iron complexes. A study of the catalytic site, bearing a triazole function resulting from the “click” chemistry, have been followed. The synthesis of a new iron-zinc complex have been then realized, with the insertion of the two metals in their destined coordination site was controlled. Insertion of a substrate inside the cavity has been realized, forming a system which could improve selectivity and efficiency of alkanes oxidation reactions.The second strategy developed was to use an electrode as source of electrons, during activation of O2 by an iron(II) complex. The cyclic voltammetry study of this reaction allowed us to reveal the formation of an adduct FeII-O2 in reductive conditions. An intermediate FeIII-peroxo was then detected at the electrode in oxidation, which generates a species with a high oxidation degree. This intermediate, generated in solution directly by reaction with H2O2, could realize oxidation reactions in oxidative conditions. New electrocatalytical systems could be then developed
Porcher, Jean-Philippe. "Synthèse de complexes bioinspirés de Mo et W catalyseurs pour la réduction des protons". Thesis, Paris 6, 2015. http://www.theses.fr/2015PA066301/document.
Enzymes containing molybdenum or tungsten within their active sites appear to be present in all form of life. Most of them are oxotransferase or hydroxylase. They contain one or two pyranopterin-dithiolene cofactor, also called Moco, in which the metal is coordinated by the dithiolene moiety. The molybdenum cofactor is highly unstable and mimicking the active site of these enzymes is challenging. A new strategy for the synthesis of a pyranopyrazine dithiolene ligand (qpdt) has been developed in our laboratory. The corresponding molybdenum complex (Bu4N)2[MoO(qpdt)2] was synthesized and characterized extensively. This unique Mo-enzyme biomimetic complex demonstrated its potential for H2 production. This complex was shown to be active for the photoreduction of protons in acidic conditions (pH = 4), in the presence of the catalyst, the photosensitizer Ru(bpy)32+, ascorbic acid in exces and gave excellent activities of 500 TON with a high stability in aqueous organic media. Moreover, the electroreduction of protons by this complex in acetonitrile showed a remarkable rate constant value of 1030 s-1 at 1.3 V. (vs Ag/AgCl). To valorize this very original ligand qpdt, (Et4N)[Ni(qpdt)2] and (Et4N)2[Co(qpdt)2]2 bisdithiolene complexes were synthesized and characterized. Preliminary studies of theses complexes have shown a potential for the photoreduction and the electroreduction of protons. These results open new directions for the search of proton reduction catalysts. This first biomimetic complex should also be exploited to understand the chemistry of this class of oxidoreductase that is still not well understood
Diao, Donglin. "Bioinspired complexes engaged within hemicryptophane cage-ligands for O2 activation and C-H bond functionalization in confined space". Electronic Thesis or Diss., Ecole centrale de Marseille, 2022. http://www.theses.fr/2022ECDM0007.
This thesis aims at developing new hemicryptophane cage-ligands to obtain confined metal-based catalysts for bioinspired O2 activation and C-H bond functionalization in confined space. The design of the targeted cages aims at introducing ligands inspired from metalloproteins active sites, for coordination of biorelevant metals (Cu, Fe, Zn). Importantly, the hemicryptophane structure provide a hydrophobic cavity around the active metal core. This structure aims at stabilizing highly reactive intermediates and reaching different reactivity compare to open model complexes, devoid of cavity. In this context, a major objective of this work was to reach Cu-based bioinspired catalysts able to activate molecular oxygen for challenging C-H bond functionalization. The first part of the thesis consists in a comprehensive literature survey on (i) background of previous applications of hemicryptophane cages and (ii) recent advances in caged bioinspired complexes. The application of our open and caged Cu-complex, based on the tris(pyridyl)amine (TPA) ligand is next described. These catalysts have been used for O2 activation and unusual intramolecular C-H bond functionalization. We then prepare and studied a new TPA-hemicryptophane cage equipped with a C(triazole)-H hydrogen bonding cavity. This functionalized cavity aims at reproducing the binding cavities found in metalloproteins. Finally, hemicryptophane cages based on the triazacyclononane (TACN) ligand have been prepared for the first time. The goal of these cage-ligands is to develop new bioinspired Cu and Fe complexes that could be, for instance, used as O2 activating catalysts
Rammal, Wassim. "Les ligands soufrés dans les métalloenzymes à cuivre : études à partir de quelques complexes modèles bioinspirés". Université Joseph Fourier (Grenoble), 2005. http://www.theses.fr/2005GRE10050.
Ln this work divided into three main parts, were studied the metal-sulphur interactions that are present in many coppel' metalloproteines by preparing various synthetic mime models of active sites of coppel' metalloproteines implicating sulphur donors in their active sites. Ln the first part the synthesis of two new tripodalligands of type N2S2 is described. Starting with these ligands, five mononuclear complexes of Cu(I) and Cu(II) were synthesized and the behaviors ofthese complexes were studied by different methods (X-ray, UV-Vis, RPE, Electrochernistry). The results showed that these complexes have a potential redox similar to those of proteins with type J copper. Ln the second part a new binuclear complex of Cu(II) ofbis (J. 1-thiolato) was prepared using a new tripodalligand N2(StBu)(SH). This mode of coordination was seldom described in literature; moreover the complete characterization of this compound is of a great interest in relation to the standard study of the centers CuA of the Cytochrome c Oxydase and the reductase of nitrous oxide. The following points were more specifically studied: i) a thorough study of the particular RPE signature ofthis cornplex, ii) the preparation using the electrochernical way and the characterization of the corresponding mixed valence species Cu(II)-Cu(I). Ln the third part for the first tirne in literature, two new dissymetric binuclear models of Cu(ll) were synthesized with the airn at understanding the role of a thioether bond which is found in the active site of the catechol oxydase which is an enzyme with type III coppel'
Domergue, Jérémy. "Modulation de l'activité SOD par contrôle de la sphère de coordination du Ni(II) dans des complexes bioinspirés". Thesis, Université Grenoble Alpes (ComUE), 2019. http://www.theses.fr/2019GREAV023.
The superoxide radical anion, O2●-, is generated by many life processes. Its radical properties make it a highly reactive species able to damage all macromolecules contributing to the pathogenesis of many diseases including neurodegenerative disorders. In order to protect cells against O2●-, Nature uses superoxide dismutases (SODs) which catalyze the dismutation of O2●- into hydrogen peroxide and oxygen. The last discovered SOD contains a nickel cofactor. Importantly the NiSOD is found in several pathogenic bacteria but not in humans. Therefore targeting the NiSOD is a promising approach to develop antibiotics. Secondly, the development of novel SOD mimics may have potential uses as therapeutic agents in oxidative stress-related diseases. Our project aims at developing innovative active NiSOD mimics, based on the use of peptide-based ligands with two main objectives: (i) to develop efficient SOD like catalysts, active in water, displaying antioxidant properties for potential therapeutic applications and (ii) to contribute to the full understanding of the catalytic mechanism of the NiSOD to highlight the specific key elements that differentiate NiSOD from the human MnSOD for the design of potential antibiotics. Our results show that, even with a coordination sphere different from the one in the enzyme, a good catalytic activity can be obtained. Key elements for the activity are also determined. Moreover, mechanistic studies indicates an inner sphere mechanism for superoxide reduction
Ségaud, Nathalie. "Étude de l'activation réductrice du dioxygène par un complexe de fer (II) et nouveaux complexes hétérodinucléaires : contributions pour le développement de catalyseurs d'oxydation bioinspirés". Phd thesis, Université Paris Sud - Paris XI, 2013. http://tel.archives-ouvertes.fr/tel-00953581.
Balasubramanian, Ramachandran. "Inversion de valence induite par le Åh dans des complexes à deux fer". Thesis, Grenoble, 2013. http://www.theses.fr/2013GRENV080/document.
The thesis matter concerns the valence inversion in FeIIFeIII induced by deprotonation of a FeII ligand. This study is of strong interest owing to the fact this process can be described as an electron transfer induced by a proton transfer. Protons and electrons transfers play essential roles in numerous catalytic or biologic reactions and therefore understanding whether they occur in a sequential or concerted manner is presently a major endeavor. The first part of the thesis is devoted to the characterization of the first system possessing this original property. It is based on binuclear complex FeIIFeIII where the two Fe ions are bridged by a dicarboxylate and a phenoxide. The ferric ion is bound by a bis-2-picolylamine group and the ferrous ion by a similar group where a pyridine has been replaced by aniline. Deprotonation of this FeII bound aniline induces the valence inversion, the resulting anilide being bound to the FeIII ion. The aniline complex was isolated with the aniline in trans position with respect to the bridging phenoxide, but it is not stable in solution and isomerizes, the aniline group moving to a cis position upon exchange with a pyridine. The same phenomenon was observed for the anilide complex obtained through deprotonation. This phenomenon was studied by combining UV-visible, 1H-RMN and Mössbauer spectroscopies, and the thermodynamic and kinetic characteristics of the isomerization were determined. The link between the electron transfer and the proton transfer were studied by electrochemical techniques. Thorough studies by cyclic voltammetry and isotopic labeling showed that in this system the electron and proton transfers are concerted. The second section of the thesis was aimed at studying the factors susceptible to influence the electron transfer, namely the redox potentials of the two Fe sites, and the proton transfer, namely the pKa of the protic ligand. To achieve it, new complexes were prepared by modifying either the protic ligand, the aniline being replaced by a benzimidazole, or the Fe binding group, substitution of bis-2-picolylamine by bis-(2-methyl-N-methylbenzimidazole)amine. Model complexes incorporating these changes but deprived of the protic ligand were also obtained to assess their influence on the redox properties of the Fe ions. The study of the influence of redox properties was considered first. The substitution of the group complexing FeIII has not a strong influence on the structure of the protonated complex which still exists as two isomers. By contrast, after deprotonation a single isomer exists. The spectroscopic properties are mostly unchanged which shows that the electronic structure of the system is not altered significantly. The study of the influence of the acidicity was then conducted. Two complexes differing by the nature of the FeIII bound group were considered. Replacing aniline by benzimidazole does not change significantly the structural properties of the system, but the valences of the Fe ions are less localized than in the original complex. The deprotonation of benzimidazole occurs and leads to a chromophore that differs from the preceding, revealing the difference in ligands. However, a preliminary electrochemical study reveals a behavior similar to that of the original complex
Gómez-Piñeiro, Rogelio Javier. "Experimental and theoretical investigation of bioinspired mononuclear copper complexes". Electronic Thesis or Diss., Aix-Marseille, 2021. http://theses.univ-amu.fr.lama.univ-amu.fr/211213_GOMEZPINEIRO_886mtbc444s58hp471nxwde_TH.pdf.
Lytic polysaccharide monooxygenases (LPMO) break down polysaccharides and are greatly studied in the context of biomass conversion. They contain a mononuclear copper center which is studied by its magnetic properties. The mechanism of reaction and its intermediates are still unknown. We use a large set of well-known complexes to develop a protocol to predict the magnetic properties of copper systems using computational calculations. This protocol was applied to LPMO models and to an LPMO-inspired tripeptidic complex to elucidate their structural and spectroscopic properties. In addition, we produced a series of complexes to capture potential high-valent reaction intermediates of LPMO. Eventually, the reactivity of one specific complex was studied for its capacity to produce formate in alcohol solvents. Formate was produced at around 120% conversion. Future generations of ligands and complexes were also synthesized and envisioned to understand the reaction pathways of LPMO
Ezzaher, Salah. "Synthèses et étude de complexes organométalliques inspirés du site actif des hydrogénases à fer seul". Brest, 2008. http://www.theses.fr/2008BRES2033.
[FeFe]H2ases are one member of the family of metalloenzymes called hydrogenases which have the ability to catalyze, with a high efficiency, both hydrogen uptake and production (2H + 2e = H2). Crystal structure determinations of the active site of iron-only hydrogenases, the H-cluster, revealed a unique organometallic assembly reminding long-known carbonyl diiron dithiolate molecules. Evidently, such a structure has inspired organometallic chemists with the task to know if it was possible to build synthetic molecules based on sulphur, iron, carbon monoxide and cyanide or surrogates, having the same efficiency as the enzyme. Some satisfactory structural models involving combinations of propanedithiolate, azadithiolate oxadithiolate or thiadithiolate and various sets of terminal ligands have been synthesized. These models were proposed in view to get a better understanding of the chemistry of the diiron active subsite and minimal structural requirements for hydrogenase activity in view of providing alternative electrocatalysts for efficient hydrogen production. No dissymetrically disubstituted species [Fe2(CO)4L2(μ-S2R)] with monodentate ligands has been reported to date. For this reason, the synthesis of unsymmetrical models requires the use of chelating ligands such as diphosphine which are able to coordinate to one metal centre in polymetallic systems. We and others started a few years ago to investigate the reactivity of hexacarbonyl diiron complexes with propanedithiolate and azadithiolate systems toward diphosphines
Libri sul tema "Complexes bioinspirés":
Weigand, Wolfgang, e Philippe Schollhammer. Bioinspired Catalysis: Metal-Sulfur Complexes. Wiley & Sons, Incorporated, John, 2014.
Weigand, Wolfgang, e Philippe Schollhammer. Bioinspired Catalysis: Metal-Sulfur Complexes. Wiley & Sons, Incorporated, John, 2014.
Weigand, Wolfgang, e Philippe Schollhammer. Bioinspired Catalysis: Metal-Sulfur Complexes. Wiley-VCH Verlag GmbH, 2014.
Weigand, Wolfgang, e Philippe Schollhammer. Bioinspired Catalysis: Metal-Sulfur Complexes. Wiley & Sons, Incorporated, John, 2014.
Weigand, Wolfgang, e Philippe Schollhammer. Bioinspired Catalysis: Metal-Sulfur Complexes. Wiley & Sons, Limited, John, 2014.
Capitoli di libri sul tema "Complexes bioinspirés":
Barrière, Frédéric. "Model Complexes of the Active Site of Nitrogenases: Recent Advances". In Bioinspired Catalysis, 225–48. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664160.ch9.
Iordache, Octavian. "Biosystems and Bioinspired Systems". In Understanding Complex Systems, 141–211. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-10654-5_4.
Garcia-Bosch, Isaac, Irene Prat, Xavi Ribas e Miquel Costas. "Bioinspired Oxidations Catalyzed by Nonheme Iron and Manganese Complexes". In Innovative Catalysis in Organic Synthesis, 27–46. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527646586.ch2.
Zouaoui, Hakima, e Abdelouahab Moussaoui. "Bioinspired Inference System for Medical Image Segmentation". In Modelling and Implementation of Complex Systems, 31–48. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-33410-3_3.
Sureshbabu, Anand Vazhapilli, Jintin Frank e Markus Zimmermann. "A Complete Workflow from Idea to Prototype for Bioinspired Design". In Design in the Era of Industry 4.0, Volume 3, 659–70. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-0428-0_54.
Jäger, Ernst-G. "“Bioinspired” Metal Complexes of Macrocyclic [N4 2-] and Open Chain [N2O2 2-] Schiff Base Ligands — a Link between Porphyrins and Salicylaldimines". In Chemistry at the Beginning of the Third Millennium, 103–38. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/978-3-662-04154-3_6.
Murahashi, Shun-Ichi, e Naruyoshi Komiya. "Bioinspired Oxidations Catalyzed by Ruthenium Complexes". In Biomimetic Oxidations Catalyzed by Transition Metal Complexes, 563–611. PUBLISHED BY IMPERIAL COLLEGE PRESS AND DISTRIBUTED BY WORLD SCIENTIFIC PUBLISHING CO., 2000. http://dx.doi.org/10.1142/9781848160699_0013.
Issac, Bini M., e S. N. Kumar. "Role of Bioinspired Optimization Algorithms in Medical Image Steganography for Healthcare Applications". In Bio-Inspired Intelligence for Smart Decision-Making, 140–58. IGI Global, 2024. http://dx.doi.org/10.4018/979-8-3693-5276-2.ch009.
Banerjee, Abhishek, Bishwajit Paul e Vijaykumar S. Marakatti. "Bioinspired Catalysis with Biomimetic Clusters". In Bioderived Materials: Harnessing Nature for Advanced Biochemical Handiwork, 39–60. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815136869124010005.
Katsuki, T. "Bioinspired Enantioselective Epoxidation Using Manganese–Salalen or Manganese–Salen Complexes as Catalyst". In Water in Organic Synthesis, 1. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-206-00059.
Atti di convegni sul tema "Complexes bioinspirés":
Abreu-Cardenas, Miguel, Saúl Calderón-Ramírez e Martín Solís. "Uncertainty Estimation for Complex Text Detection in Spanish". In 2023 IEEE 5th International Conference on BioInspired Processing (BIP). IEEE, 2023. http://dx.doi.org/10.1109/bip60195.2023.10379278.
Madrenas, Jordi, e J. Manuel Moreno. "Strategies in SIMD Computing for Complex Neural Bioinspired Applications". In 2009 NASA/ESA Conference on Adaptive Hardware and Systems (AHS). IEEE, 2009. http://dx.doi.org/10.1109/ahs.2009.31.
Lopez-De-Ipina, Karmele, Nora Barroso, Pilar M. Calvo, Aitzol Ezeiza e Carmen Hernandez. "A Multilingual System Based on Semantic Knowledge for Complex Environments". In 2018 IEEE International Work Conference on Bioinspired Intelligence (IWOBI). IEEE, 2018. http://dx.doi.org/10.1109/iwobi.2018.8464207.
Marcello, Javier, Dionisio Rodriguez-Esparragon, Edurne Ibarrola-Ulzurrun e Consuelo Gonzalo-Martin. "Multisensor fusion for the accurate classification of vegetation in complex ecosystems". In 2019 IEEE International Work Conference on Bioinspired Intelligence (IWOBI). IEEE, 2019. http://dx.doi.org/10.1109/iwobi47054.2019.9114397.
Romero-Sandoval, Mario, Saúl Calderón-Ramírez e Martín Solís. "Using GPT-3 as a Text Data Augmentator for a Complex Text Detector". In 2023 IEEE 5th International Conference on BioInspired Processing (BIP). IEEE, 2023. http://dx.doi.org/10.1109/bip60195.2023.10379347.
Song, Young Min. "Artificial vision systems inspired by the eyes of aquatic animals". In CLEO: Applications and Technology. Washington, D.C.: Optica Publishing Group, 2023. http://dx.doi.org/10.1364/cleo_at.2023.jth3e.4.
Zhang, Xun, Lei Wang, Lubin Wang e Liang Li. "Bioinspired Motion Information Guided Tracking Algorithm for Small Targets in Infrared Images". In 2023 International Annual Conference on Complex Systems and Intelligent Science (CSIS-IAC). IEEE, 2023. http://dx.doi.org/10.1109/csis-iac60628.2023.10363835.
Hooper, Joshua, Andy Houghton e Ayse Tekes. "Bioinspired Monolithically Designed Compliant Swimming Robots". In ASME 2020 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/imece2020-23321.
Casas, María J., e Francisco J. Vico. "On the performance of some bioinspired genetic operators in complex structures evolution". In the 11th Annual conference. New York, New York, USA: ACM Press, 2009. http://dx.doi.org/10.1145/1569901.1570193.
Yang, Chunyu, Yaohan Tang, Linna Zhou e Xiaoping Ma. "Complete Coverage Path Planning Based on Bioinspired Neural Network and Pedestrian Location Prediction". In 2018 IEEE 8th Annual International Conference on CYBER Technology in Automation, Control, and Intelligent Systems (CYBER). IEEE, 2018. http://dx.doi.org/10.1109/cyber.2018.8688311.
Rapporti di organizzazioni sul tema "Complexes bioinspirés":
Doyle, John. Bioinspired Concepts: Unified Theory for Complex Biological and Engineering Systems. Fort Belvoir, VA: Defense Technical Information Center, gennaio 2006. http://dx.doi.org/10.21236/ada484230.
Doyle, John C. Bioinspired Concepts: Unified Theory for Complex Biological and Engineering Systems. Fort Belvoir, VA: Defense Technical Information Center, gennaio 2001. http://dx.doi.org/10.21236/ada434182.
Buehler, Markus J. Differential Multiscale Modeling of Chemically Complex Materials under Heavy Deformation: Biological, Bioinspired and Synthetic Hierarchical Materials. Fort Belvoir, VA: Defense Technical Information Center, giugno 2010. http://dx.doi.org/10.21236/ada533318.