Relevant bibliographies by topics / Molecular materials

Academic literature on the topic 'Molecular materials'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 March 2023

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Journal articles on the topic "Molecular materials"

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Miller, J. S. "Molecular Materials." Science 262, no. 5138 (November 26, 1993): 1460. http://dx.doi.org/10.1126/science.262.5138.1460.

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Miller, Joel S. "Molecular Materials I. Molecular materials mimic inorganic network solids." Advanced Materials 2, no. 2 (February 1990): 98–99. http://dx.doi.org/10.1002/adma.19900020207.

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Harada, Akira, and Mikiharu Kamachi. "Molecular Assembly Materials." Kobunshi 41, no. 12 (1992): 814–17. http://dx.doi.org/10.1295/kobunshi.41.814.

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Coronado, E., A. Forment-Aliaga, J. R. Galán-Mascarós, C. Giménez-Saiz, C. J. Gómez-Garcı́a, E. Martinéz-Ferrero, A. Nuez, and F. M. Romero. "Multifunctional molecular materials." Solid State Sciences 5, no. 6 (June 2003): 917–24. http://dx.doi.org/10.1016/s1293-2558(03)00116-x.

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Gatteschi, Dante. "Magnetic molecular materials." Current Opinion in Solid State and Materials Science 1, no. 2 (April 1996): 192–98. http://dx.doi.org/10.1016/s1359-0286(96)80083-0.

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Dei, Andrea. "Magnetic molecular materials." Inorganica Chimica Acta 191, no. 2 (January 1992): 279. http://dx.doi.org/10.1016/s0020-1693(00)93471-6.

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Andruh, Marius. "Inorganic molecular materials." Comptes Rendus Chimie 15, no. 10 (October 2012): 837. http://dx.doi.org/10.1016/j.crci.2012.10.001.

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Chorazy (Guest Editor), Szymon, and Barbara Sieklucka (Guest Editor). "Functional Molecular Materials." Open Chemistry Journal 6, no. 1 (March 22, 2019): 8–9. http://dx.doi.org/10.2174/1874842201906010008.

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Xu, Jialiang, Chengfen Xing, and Xian-He Bu. "Functional molecular materials." Chinese Chemical Letters 29, no. 2 (February 2018): 217–18. http://dx.doi.org/10.1016/j.cclet.2018.01.009.

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Ouahab, Lahcène, and Toshiaki Enoki. "Multiproperty Molecular Materials: TTF-Based Conducting and Magnetic Molecular Materials." European Journal of Inorganic Chemistry 2004, no. 5 (March 2004): 933–41. http://dx.doi.org/10.1002/ejic.200300869.

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Dissertations / Theses on the topic "Molecular materials"

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Souto, Salom Manuel. "Multifunctional Materials based on TTFPTM dyads: towards new Molecular Switches, Conductors and Rectifiers." Doctoral thesis, Universitat Autònoma de Barcelona, 2016. http://hdl.handle.net/10803/393986.

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Esta Tesis está centrada en el diseño, síntesis y caracterización de nuevos materiales moleculares multifuncionales basados en sistemas Dador-Aceptor (D-A) formados por la unidad dadora de electrones tetratiafulvaleno (TTF) enlazada a la unidad aceptora de electrones el radical policlorotrifenilmetilo (PTM) mediante diferentes puentes -conjugados. Estos compuestos pueden exhibir propiedades físicas muy interesantes como biestabilidad o propiedades ópticas no lineales en solución, conductividad en estado sólido o rectificación cuando son anclados en superficies. Por tanto, estos sistemas podrían encontrar aplicación en el campo de la electrónica molecular como interruptores, conductores o rectificadores. En la primera parte de esta Tesis, se estudiará el fenómeno de biestabilidad en solución de un sistema D-A basado en un radical PTM conectado a un TTF mediante un puente vinileno. Este sistema puede exhibir un cambio inducido por la temperatura entre dímeros diamagnéticos a temperatura ambiente y monómeros paramagnéticos a alta temperatura. Los dos distintos estados presentan diferentes propiedades ópticas y magnéticas utilizando la temperatura como estímulo externo. Por otra parte, también se presentará el diradical A-D-A compuesto por dos subunidades PTM radicalarias conectadas mediante un puente TTF-vinileno que puede modificar reversiblemente sus propiedades ópticas, magnéticas y electrónicas al oxidarse o reducirse en solución. La modificación de la deslocalización electrónica y del acoplamiento magnético se observa cuando generamos las especies cargadas y los cambios han sido racionalizados mediante cálculos teóricos. En la segunda parte de la Tesis, se presentará la síntesis y caracterización de distintos derivados TTF--PTM incrementando el número de vinilenos entre las unidades D y A. También se estudiará la transferencia de carga intramolecular y las propiedades ópticas no lineales (NLO) en solución y su dependencia con la estructura electrónica abierta así como con la longitud del puente de cada uno de los compuestos. En la tercera parte de la Tesis, se estudiará las arquitecturas auto-ensambladas en estado sólido de un nuevo sistema TTF-PTM. La estructura cristalina muestra un ordenamiento supramolecular con una segregación de las unidades dadoras y aceptoras. Además, se estudiará la aparición de conductividad en los cristales del mismo sistema al aumentar la presión. El comportamiento de semiconductor a altas presiones se relacionará con el aumento de interacciones intermoleculares así como con el incremento de la deslocalización de carga. Finalmente, en la última parte de la Tesis se presentará un nuevo compuesto TTF-PTM que ha sido funcionalizado con un grupo disulfuro para preparar monocapas auto-ensambladas (SAMs) en superficies de oro. Estas SAMs han sido caracterizadas mediante diversas técnicas espectroscópicas para estudiar la estructura electrónica del sistema. Además, se estudiará el transporte de carga a través de las SAMs para evaluar un posible comportamiento de rectificación.
This Thesis is focused on the design, synthesis and characterization of new multifunctional molecular materials based on donor-acceptor (D-A) dyads formed by the electron-donor tetrathiafulvalene (TTF) unit linked to the electron-acceptor polychlorotriphenylmethyl (PTM) radical moiety through different -conjugated bridges. These compounds can exhibit interesting physical properties such bistability and nonlinear optical properties in solution, conductivity in the solid state or electrical rectification when anchored on surfaces. Thus, these systems could find potential applications in the field of molecular electronics as switches, conductors or rectifiers. In the first part of the Thesis, we have studied the bistability phenomenon in solution of a D-A dyad based on a PTM radical linked to a TTF moiety through a vinyelene bridge. This system exhibited a temperature-induced switching between diamagnetic dimers at room temperature and paramagnetic monomers at high temperature. The two different states showed different optical and magnetic properties when using the temperature as external input. On the other hand, we have also reported the A-D-A diradical triad based on two PTM radical subunits connected through a TTF-vinylene bridge that can reversibly modify the optical, electronic and magnetic properties by one-electron reduction and oxidation in CH2Cl2 solution. The modification of electron delocalization and magnetic coupling was observed when the charged species were generated and the changes were rationalized by theoretical calculations. In the second part of the Thesis, we have reported the synthesis and characterization of different TTF--PTM dyad derivatives increasing the number of vinylene units between the D and A moieties. We have studied the intramolecular charge transfer and non-linear optical (NLO) properties in solution and their dependence on the open-shell structure as well as on the bridge length for this family of compounds. In the third part of the Thesis, we have studied self-assembled architectures in the solid state of a new D-A dyad based on a PTM radical linked to a TTF moiety through a -phenyl-pyrrole bridge. The crystal structure showed an interesting supramolecular arrangement with segregated donor and acceptor units. Moreover, we reported the appearance of conductivity in single crystals of the same system when increasing the pressure. The semiconducting behavior at high pressures has been attributed to the enhanced intermolecular interactions and charge delocalization due to incorporation of TTF units which force the formation of close packed stacks of molecules. Finally in the last part of the Thesis, we have reported a new TTF-PTM dyad that was functionalized with a disulfide group in order to prepare self-assembled monolayers (SAMs) on gold. These SAMs were fully characterized by different spectroscopic techniques in order to study the electronic structure of the system. Moreover, charge transport measurements through the SAMs were performed in order to evaluate the possible rectification behavior.
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Villabona, Pedemonte Marc. "Photofunctional processes and materials based on molecular switches." Doctoral thesis, Universitat Autònoma de Barcelona, 2021. http://hdl.handle.net/10803/673837.

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Els interruptors moleculars han estat un camp de recerca important en els últims anys degut a la seva capacitat per interconvertir-se entre múltiples estats al estar exposats a un estímul (escriptura) i al fet de modificar les seves propietats després del canvi (lectura). Els interruptors moleculars que interaccionen amb llum per canviar d’estat o bé que modifiquen les seves propietats òptiques són d’especial interès ja que la llum permet un alt control espai temporal de forma no invasiva i la seva detecció té una alta sensibilitat. Per aquest motiu, durant aquesta tesis s’han desenvolupat múltiples materials i processos fotofuncionals els quals poden resumir-se en dues parts: Per una banda, el caràcter multiestat d’una família de interruptors molecular (fluoro)cròmics basats en compostos espirocíclics zwitteriònics de Meisenheimer (SZMC), es va ampliar mitjançant la identificació d’un nou estat catiònic amb propietats òptiques distintives, el qual és pot generar tant electroquímicament com a través de l’adició d’un àcid. A més, es va investigar el comportament termo(fluoro)cròmic dels SZMC i es va demostrar que podien respondre tant a canvis en el dissolvent com a la presència d’anions. Aquest comportament multiestat i de resposta a múltiples estímuls va ser emprat en la preparació de una sèrie de materials fotofuncionals basats en SZMC com: un detector de pH d’ampli espectre, dispositius electro(fluoro)cròmics i sensors iònics, termals i de dissolvents. Per altra banda, es van controlar tres processos químics amb ditieniletens (DTE) mitjançant llum. Primer, la introducció d’un grup electroacceptor EWG va permetre la modulació del pKa de fenols funcionalitzats amb DTEs. Després, el control amb dues longituds d’ona d’una reacció d’amidació es va aconseguir amb un estratègia similar a l’anterior utilitzant un éster activat basat en DTE. Aquest va reaccionar fins a 24 vegades més ràpid en el estat tancat generat amb llum UV (ie. activació amb UV) que amb l’estat obert obtingut sota irradiació amb llum visible (ie. desactivació amb visible). Finalment, la estratègia de controlar reaccions amb dos colors també va ser aplicada en la fotoligació mitjançant una reacció de oxo-Diels Alder d’un dienòfil basat en DTE actiu en la forma tancada (ie. Activacióamb llum UV, desactivació amb llum visible) i un diè generat en llum UV basat en orto-metilbenzaldèhid.
Los interruptores moleculares han sido un campo de investigación importante en los últimos años debido a la capacidad de interconvertir-se entre múltiples estados al exponerse a un estímulo (escritura) y modificar sus propiedades (lectura). De especial interés han sido los interruptores moleculares que interaccionan con la luz ya sea para cambiar de estado o bien modificar sus propiedades ópticas en la transformación. Esto és debido a que la luz permite un alto control espaciotemporal al mismo tiempo que és no invasiva y altamente sensible a la detección. Por estos motivos, durante esta tesis se han desarrollados múltiples materiales y procesos fotofuncionales los cuales pueden resumirse en dos partes: Por un lado, el carácter multiestado de una familia de interruptores moleculares (fluoro)crómicos basados en compuestos espirocíclicos zwitteriònicos de Meisenheimer (SZMC) se amplió mediante la identificación de un nuevo estado catiónico, con propiedades ópticas distintivas, que se puede generar tanto electroquímicamente, como a través de la adición de ácido. Además, se investigó el comportamiento termo(fluoro)crómico de los SZMC y se demostró que podían responder tanto a cambios en el disolvente como a la presencia de iones. Este comportamiento multiestado i de respuesta a múltiples estímulos fue utilizado en la preparación de varios materiales fotofuncionales basados en SZMC como: un detector de pH de amplio espectro, dispositivos electro(fluoro)crómicos i sensores iónicos, termales i de disolventes. Por otro lado, se controlaron tres procesos químicos diferentes con interruptores moleculares fotoinducidos de tipo ditienileteno (DTE) mediante luz. Primero, la introducción de un grupo electroacceptor permitió la modulación del pKa de un fenol funcionalizado con un DTE. Segundo el control de una reacción de amidación con dos longitudes de onda fue conseguido con una estrategia similar a la anterior utilizando un ester activado basado en DTE. Este reacciona hasta 24 veces más rápido en el estado cerrado generado con luz ultravioleta (ie. activación con UV) que en el estado abierto que se obtiene al irradiar con luz visible (ie. desactivación con visible). Finalmente, el control de reacciones con dos colores de luz fue utilizado para controlar la reacción de oxo-Diels Alder entre un dienófilo basado en DTE activo en el estado cerrado (ie. activación con UV, desactivación con luz visible) i un dieno generado con luz UV basado en orto-metilbenzaldehido.
Molecular switches have been an important research field in the recent years due to its capacity to interconvert between multiple states through a stimulus (writing) and change their properties (reading). Of special interest are molecular switches that interact with light by either changing their optical properties or reacting as stimulus, due to its noninvasive high spatiotemporal control and sensitivity. As a result, several photofunctional materials and processes based on molecular switches were developed during this thesis which can be summarized in two topics. On the one hand, the multistate character of a family of (fluoro)chromic molecular switches based on spirocyclic zwitterionic Meisenheimer compounds (SZMC) was broadened by identifying a novel cationic state with distinctive optical properties, which could be achieved electrochemically or via acid addition. Moreover, the thermo(fluoro)chromic behavior of SZMCs was investigated and successfully demonstrated that they can respond to certain ions and solvents. This multistimuli-responsive and multistate character was then exploited for the preparation of a variety of photofunctional materials based on SZMCs: wide-range pH detectors, electro(fluoro)chromic displays, and thermal, ionic and solvent sensors. On the other hand, light controlled reactivity with dithienylethenes (DTE) was achieved for three chemical processes. First, the introduction of electrowithdrawing groups (EWG) allowed the modulation of the pKa in acetonitrile of a series of DTEs tethering phenol moieties. Second, a similar strategy allowed for the dual-color control of an amidation reaction employing DTE-based active esters which react up to 24 times faster in the UV-generated closed state (ie. activation with UV irradiation) than in the open state formed under visible illumination (ie depletion with visible light). Finally, two-wavelength control was also achieved for an oxo-Diels Alder reaction between a DTE-dienophile active in the closed state and a UV-generated diene based on orto-methylbenzaldehyde.
Universitat Autònoma de Barcelona. Programa de Doctorat en Química
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Qian, Wenjie. "Preparation and processing of molecular materials with optoelectronic properties." Doctoral thesis, Universitat Autònoma de Barcelona, 2018. http://hdl.handle.net/10803/664220.

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Materiales orgánicos basados en moléculas pequeñas con propiedades optoelectrónicas son particularmente atractivos en los campos de celdas solares orgánicas y en el campo de la electrónica molecular. Porfirinas y curcuminoides (CCMoids) son moléculas que suscitan interés, siendo buenas candidatas en los campos mencionados, debido a que presentan estructuras químicas modificables y excelentes propiedades electrónicas. En esta tesis, se han estudiado la preparación y diseño de moléculas pertenecientes a las dos familias aquí indicadas, la capacidad de autoensamblaje de dichas moléculas conjuntamente con sus posibles aplicaciones. En el capítulo II, se han sintetizado dos metaloporfirinas (Zn(4R-PPP) y Zn(PPP)) ligandos largos que contienen centros quirales o aquirales conjutantemente con grupos carbonilos en las cuatro posiciones meso de sus respectivos núcleos de porfirina. Posteriorment, se ha sintetizado un estudio completo relacionado con las interacciones intermoleculares no covalentes de dichas multiporfirinas y experimentos iniciales con la creación de celdas solares orgánicas de hetero-unión (BHJ-OCs) donde este tipo de porfirinas han sido procesadas en solución para el estudio de su comportamiento como sistemas donadores en dichas celdas. Dicho estudio se extendió en el capítulo III a dos nuevas porfirinas (TEP y Zn (TEP)) con sustituyentes carbonilos pero más cortos donde se investigó el efecto de las dimensiones de los ligandos en las interacciones intermoleculares finales, y cómo esto afecta el rendimiento de OSCs. En el capítulo IV se explica como con los mismos centros quirales en las posiciones meso, se obtuvo una nueva porfirina, Zn(4R-CPP), que contiene grupos carboxílicos. También se muestran los estudios con dicho sistema y porfirinas adicionales con la formación de sistemas de autoensamblaje binarios basados en interacciones no covalentes o de autoensamblaje iónico para su posible aplicación como nanomateriales. En el Capítulo V, se sintetizaron CCMoides que contienen grupos quirales, de forma similar al capítulo II, así como el estudio del efecto de la quiralidad de dichos materiales. Además, la investigación hace énfasis en el logro de grupos ácidos terminales a partir de la hidrolización de los grupos ésteres (como se muestra en el capítulo IV) que permitió investigar la posible creación de sistemas con diferente dimensionalidades. Después, en el Capítulo VI, se exploró la síntesis de CPs /redes mediante el uso de CCMoides que contienen grupos piridínicos en sus terminaciones (3Py-CCM). El último capítulo está dedicado al diseño de nuevos derivados de porfirina que contienen grupos de anclaje basados en azufre para su aplicación en electrónica molecular conjuntamente con el estudio de sus propiedades electrónicas en solución y en estado sólido. Además, una familia de CCMoids también se ha analizado de manera similar a los derivados de porfirina, con el objetivo de recopilar información para mejorar su diseño molecular para aplicaciones electrónicas.
Organic small molecules materials with optoelectronic properties are particularly attractive in the fields of organic solar cells and molecular electronics. Porphyrins and curcuminoids (CCMoids) are prospective candidates in these fields due to their modifiable chemical structures and outstanding properties. In this thesis, the design and preparation of these two families of molecules, together with their self-assembly abilities and potential applications have been studied. In chapter II, two metalloporphyrins (Zn(4R-PPP) and Zn(PPP)) containing long chiral or achiral moieties with carbonyl substituents in the four meso-positions of their porphyrin cores have been synthesized. Then, a complete study related to non-covalent multiporphyrin assemblies has been performed, and initial solution-processed bulk heterojunction organic solar cell experiments were presented. To extend the above study, in chapter III, new porphyrins (TEP and Zn(TEP)) with shorter carbonyl substituents have been investigated and the effect of the length of the ligands in intermolecular interactions was studied, searching how this factor affects as well the OSCs performance. With the same chiral centres in the meso-positions, a porphyrin Zn(4R-CPP) involving carboxylic groups was obtained in chapter IV. And the binary self-assembling systems based on its derivations were achieved through non-covalent interaction or ionic self-assembly towards their potential application as active components in nanomaterials. In Chapter V, CCMoids containing chiral groups, in a similar manner as chapter II, were synthesized. In addition, research towards the achievement of terminal acid groups from the hydrolyzation of the ester groups (as chapter IV shows) allowed the investigation of the possible creation of systems with different dimensionalities. Then in Chapter VI, the synthesis of CPs/networks was explored by the use of a CCMoid containing pyridine moieties at its endings (3Py-CCM). The last chapter is devoted to the design of new porphyrin derivatives containing sulphur-based anchoring groups for their application in single molecular electronics together with the study of their electronic properties in solution and solid state. In addition, a family of CCMoids has also been analysed in a similar manner as the porphyrin derivatives, with the aim of gathering information to improve their molecular design for electronic applications.
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Saraf, Sanjeev R. "Molecular characterization of energetic materials." Texas A&M University, 2003. http://hdl.handle.net/1969.1/331.

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Assessing hazards due to energetic or reactive chemicals is a challenging and complicated task and has received considerable attention from industry and regulatory bodies. Thermal analysis techniques, such as Differential Scanning Calorimeter (DSC), are commonly employed to evaluate reactivity hazards. A simple classification based on energy of reaction (-H), a thermodynamic parameter, and onset temperature (To), a kinetic parameter, is proposed with the aim of recognizing more hazardous compositions. The utility of other DSC parameters in predicting explosive properties is discussed. Calorimetric measurements to determine reactivity can be resource consuming, so computational methods to predict reactivity hazards present an attractive option. Molecular modeling techniques were employed to gain information at the molecular scale to predict calorimetric data. Molecular descriptors, calculated at density functional level of theory, were correlated with DSC data for mono nitro compounds applying Quantitative Structure Property Relationships (QSPR) and yielded reasonable predictions. Such correlations can be incorporated into a software program for apriori prediction of potential reactivity hazards. Estimations of potential hazards can greatly help to focus attention on more hazardous substances, such as hydroxylamine (HA), which was involved in two major industrial incidents in the past four years. A detailed discussion of HA investigation is presented.
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Miller, Paul Francis. "Luminescence studies of molecular materials." Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342250.

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Aricó, Fabio. "New architectures for molecular materials." Thesis, University of Reading, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252257.

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Allan, Margaret Lucy. "Magnetic interactions in molecular materials." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387026.

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Staniland, Sarah S. "Sulphur-rich molecular magnetic materials." Thesis, University of Edinburgh, 2005. http://hdl.handle.net/1842/12990.

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The work within this thesis is concerned with several different magnetic systems all involving materials that are rich in sulphur and are thus predicted to have strong magnetic coupling through these sulphur atoms. Firstly, a range of molecular salt materials of [dithiazolyl]x[M(dithiolene)2] were synthesised and their magnetic behaviour analysed. Dithiolene complex salts of [BDTA]+ [2]-[6] were found to have a mainly mixed anion-cation stacked structural motif and show a number of interesting magnetic properties, such as an almost perfect one dimensional antiferromagnetic chain system ([BDTA]2[Cu(mnt)2 [2], as well as the conducting charge transfer salt [BDTA][Ni(dmit)2]2 [3] that is the first example of the [BDTA]+ cation behaving as an open shell cation. The [BDTA]2[Fe(tdas)2Cl] salt [5] has the first mixed stacking structural motif of this anion (as it usually dimerises) and this material was found to be paramagnetic. The paramagnetic radical dithiazolyl cation [BBDTA]+ was also co-precipitated with dithiolene complexes to create magnetic salts [11]-[15]. These all showed mixed magnetic effects with some unusual magnetic interactions occurring. [BDTA]+ was also co-crystallised with MC142- anions to form molecular materials containing two dimensional magnetic structure with a square lattice magnetic pathway. This magnetic mechanism provides ideal materials for the study of ground state quantum magnetic effects that are thought to be related to the fundamental mechanism of superconductivity. This work also contains the study of the non interacting magnetic molecular thiophosphine complexes of the form [M((SPR1R2)2N)2] (M = Mn, Co, Ni, R1 = R2 = Ph, iPr and R1=Ph and R2=iPr) which behave as simple paramagnets ([16]-[24]). All M = Mn and Co complexes were found to be simple paramagnetic materials with a strong ligand field splitting.
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Branton, Philip Michael. "Molecular design of inorganic materials." Thesis, University of Surrey, 1998. http://epubs.surrey.ac.uk/844618/.

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Work on modelling compounds possessing die tetraaza[14]annulene (TAA) fragment is described. Modelling studies have been conducted to investigate both structural and electronic properties, of both single molecules and extended arrays of these compounds. The structural aspects have been investigated using molecular mechanics and crystallographic database investigations. Molecules based on the tetraaza[14] annulene structure have been found to adopt one of four conformations. The geometries of these conformations are planar, saddle-shaped, slightly twisted, and dome-shaped. The complexed metal centre and the arrangement of substituents on the periphery of the ligand, have been found to determine which conformation a molecule adopts. In order to model the compounds, three new atom types have been created for the Universal Force Field. The electronic aspects have been investigated using Hartree Fock based calculations for single molecules and Extended Huckel based calculations for extended systems. The electronics of die single molecules have shown there to be a linear trend in the LUMO energies, although die HOMO energies vary very little. The reason for this trend in the LUMOs is unknown, but appears not to be related to any obvious structural feature.
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Warrell, Rachel Marie. "Synthetic and Conformational Studies in Molecular Encapsulation with a Twisted Molecular Basket Complexing Organophosphorus Molecules and Fentanyl Analogues." The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1502899516087168.

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Books on the topic "Molecular materials"

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Bruce, Duncan W., Dermot O'Hare, and Richard I. Walton, eds. Molecular Materials. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470686058.

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Bruce, Duncan W., Dermot O'Hare, and Richard I. Walton. Molecular materials. Hoboken, N.J: Wiley, 2010.

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Molecular materials. Hoboken, N.J: Wiley, 2010.

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Sieklucka, Barbara, and Dawid Pinkowicz, eds. Molecular Magnetic Materials. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527694228.

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Gatteschi, Dante, Olivier Kahn, Joel S. Miller, and Fernando Palacio, eds. Magnetic Molecular Materials. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3254-1.

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NATO Advanced Research Workshop on Magnetic Molecular Materials (1990 Il Ciocco, Italy). Magnetic molecular materials. Dordrecht: Kluwer Academic Publishers, 1991.

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Gatteschi, D. Magnetic Molecular Materials. Dordrecht: Springer Netherlands, 1991.

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Saito, Gunzi, Fred Wudl, Robert C. Haddon, Katsumi Tanigaki, Toshiaki Enoki, and Howard E. Katz, eds. Multifunctional Conducting Molecular Materials. Cambridge: Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847557605.

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Jiang, Jianzhuang, ed. Functional Phthalocyanine Molecular Materials. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-04752-7.

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service), SpringerLink (Online, ed. Functional Phthalocyanine Molecular Materials. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2010.

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Book chapters on the topic "Molecular materials"

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Winpenny, Richard E. P., and Eric J. L. McInnes. "Molecular Nanomagnets." In Molecular Materials, 281–348. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470686058.ch5.

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Robertson, Neil, and Gordon T. Yee. "Molecular Magnetic Materials." In Molecular Materials, 143–209. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470686058.ch3.

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Gatteschi, Dante, Andrea Caneschi, and Roberta Sessoli. "Magnetic Molecular Materials." In Inorganic and Organometallic Polymers with Special Properties, 147–60. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2612-0_11.

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Lee, Charles Y. C., and Larry Dalton. "Molecular Engineering." In Photoactive Organic Materials, 543–46. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-017-2622-1_38.

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Ghosh, Subhasis. "Molecular Electronics." In Advanced Structured Materials, 235–60. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-6214-8_9.

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Mathonière, Corine, Hiroko Tokoro, and Shin-ichi Ohkoshi. "Molecular Photomagnets." In Molecular Magnetic Materials, 323–44. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694228.ch13.

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Palstra, Thomas T. M., and Alexey O. Polyakov. "Molecular Multiferroics." In Molecular Magnetic Materials, 405–18. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694228.ch16.

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Shatruk, Michael, Silvia Gómez-Coca, and Kim R. Dunbar. "Molecular Magnetism." In Molecular Magnetic Materials, 29–51. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694228.ch2.

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Maury, Olivier, and Hubert Le Bozec. "Metal-Based Quadratic Nonlinear Optical Materials." In Molecular Materials, 1–59. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470686058.ch1.

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Binnemans, Koen. "Physical Properties of Metallomesogens." In Molecular Materials, 61–141. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470686058.ch2.

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Conference papers on the topic "Molecular materials"

1

Omatsu, Takashige. "Light induced chiral structured materials (Conference Presentation)." In Molecular Machines, edited by Zouheir Sekkat. SPIE, 2018. http://dx.doi.org/10.1117/12.2323650.

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Takashima, Yoshinori, and Akira Harada. "Photo-stimuli responsive supramolecular materials using supramolecular machine." In Molecular Machines, edited by Zouheir Sekkat. SPIE, 2018. http://dx.doi.org/10.1117/12.2322130.

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P. Tarakeshwar, Juan Jose Palacios, and Dae M. Kim. "Electrode-molecule interface effects on molecular conductance." In 2006 IEEE Nanotechnology Materials and Devices Conference. IEEE, 2006. http://dx.doi.org/10.1109/nmdc.2006.4388726.

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Shelton, David P. "Scaling Law For Molecular Hyperpolarizabilities." In Nonlinear Optical Properties of Materials. Washington, D.C.: Optica Publishing Group, 1988. http://dx.doi.org/10.1364/nlopm.1988.mb2.

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Bosshard, Christian. "Organic Nonlinear Optical Materials." In The European Conference on Lasers and Electro-Optics. Washington, D.C.: Optica Publishing Group, 1998. http://dx.doi.org/10.1364/cleo_europe.1998.ctuj2.

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Abstract:
Organic materials hold a large promise for second- and third-order nonlinear optical and fast electro-optic applications due to the large nonlinearities of the basic molecular units and the almost purely electronic origin of the nonlinearity. We here discuss the new development in this field with respect to molecules, polymers, and molecular crystals.
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Lee, H., and M. H. Jung. "Molecular Memory Nano-interfaced with Organic Molecules." In 2010 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2010. http://dx.doi.org/10.7567/ssdm.2010.a-4-1.

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Castaño, V. M., J. García-Macedo, A. Mondragón, and R. Rodríguez. "Molecular engineering of optical materials." In CAM-94 Physics meeting. AIP, 1995. http://dx.doi.org/10.1063/1.48805.

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Asselberghs, Inge, Gunther Hennrich, Jon McCleverty, Leila Boubekeur-Lecaque, Benjamin J. Coe, and Koen Clays. "Organic materials for molecular switching." In Photonics Europe, edited by Paul L. Heremans, Michele Muccini, and Eric A. Meulenkamp. SPIE, 2008. http://dx.doi.org/10.1117/12.779751.

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Wu, Si. "Near-infrared light-controlled soft materials based on upconversion (Conference Presentation)." In Molecular Machines, edited by Zouheir Sekkat. SPIE, 2018. http://dx.doi.org/10.1117/12.2321074.

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Balabaev, Nikolay K., Alexander L. Rabinovich, and Pauli O. Ripatti. "Molecular dynamics simulations of isolated molecules of polyunsaturated lipids." In International Workshop on New Approaches to High Tech Materials: Nondestructive Testing and Computer Simulations in Materials Scienc, edited by Alexander I. Melker. SPIE, 1998. http://dx.doi.org/10.1117/12.299597.

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Reports on the topic "Molecular materials"

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Bayley, Hagan. Molecular Genetic Approaches to Biomolecular Materials. Fort Belvoir, VA: Defense Technical Information Center, November 2000. http://dx.doi.org/10.21236/ada391351.

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Freed, Karl F. Towards the Molecular Design of Composite Materials. Fort Belvoir, VA: Defense Technical Information Center, January 1998. http://dx.doi.org/10.21236/ada361070.

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Freed, Karl F. Towards the Molecular Design of Composite Materials. Fort Belvoir, VA: Defense Technical Information Center, February 1994. http://dx.doi.org/10.21236/ada283422.

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Bohn, Paul W., and Jonathan V. Sweedler. Three Dimensional Molecular Imaging for Lignocellulosic Materials. Office of Scientific and Technical Information (OSTI), June 2011. http://dx.doi.org/10.2172/1043043.

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Reilly, Dallas D. Molecular Forensic Science Analysis of Nuclear Materials. Office of Scientific and Technical Information (OSTI), October 2012. http://dx.doi.org/10.2172/1053139.

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Jia, S., T. M. Nenoff, P. Provencio, Y. Qiu, J. A. Shelnutt, S. G. Thoma, and J. Zhang. Design Molecular Recognition Materials for Chiral Sensors, Separtations and Catalytic Materials. Office of Scientific and Technical Information (OSTI), November 1998. http://dx.doi.org/10.2172/2055.

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Thies, Mark C. The Molecular Design of High-Performance Carbon Materials. Fort Belvoir, VA: Defense Technical Information Center, June 2008. http://dx.doi.org/10.21236/ada488341.

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Furche, Filipp, Shane M. Parker, Mikko J. Muuronen, and Saswata Roy. Non-Adiabatic Molecular Dynamics Methods for Materials Discovery. Office of Scientific and Technical Information (OSTI), April 2017. http://dx.doi.org/10.2172/1351540.

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Struzhkin, Viktor V., Wendy L. Mao, Ho-Kwang Mao, Burkhard Militzer, and Russell Hemley. Hydrogen Storage in Novel Molecular Materials, Final Report. Office of Scientific and Technical Information (OSTI), May 2006. http://dx.doi.org/10.2172/977587.

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Phillips, N. E., R. H. Muller, and C. V. Peterson. Materials and Molecular Research Division: Annual report, 1986. Office of Scientific and Technical Information (OSTI), July 1987. http://dx.doi.org/10.2172/6253859.

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