Log in

Relevant bibliographies by topics / Inorganic-organic hybrid compounds

Contents

Journal articles
Dissertations / Theses
Books
Book chapters
Conference papers

Academic literature on the topic 'Inorganic-organic hybrid compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Inorganic-organic hybrid compounds.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Inorganic-organic hybrid compounds"

1

Matsui, Takashi, Mitsuyasu Kawahara, Kenjiro Teshima, Masahiro Rikukawa, and Kohei Sanui. "Novel Organic-Inorganic Hybrid Compounds Containing Alkyldiammonium Salts." Molecular Crystals and Liquid Crystals 376, no. 1 (January 1, 2002): 89–94. http://dx.doi.org/10.1080/713738452.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Luo, Dawei, Jian Zhang, Yu Liang, Jianling Ni, Fangming Wang, and Wei Liu. "New Copper Bromide Organic-Inorganic Hybrid Molecular Compounds with Anionic Inorganic Core and Cationic Organic Ligands." Crystals 12, no. 1 (December 23, 2021): 19. http://dx.doi.org/10.3390/cryst12010019.

Full text

Abstract:

Here, organic-inorganic hybrid molecular compounds based on copper(I) bromide have been synthesized by slow-diffusion method. The inorganic modules of these two structures are Cu2Br42− anion, and the inorganic modules are coordinated to cationic organic ligands via Cu-N coordinative bonds. Both of these compounds are luminescent, emitting green emissions under UV excitation.

APA, Harvard, Vancouver, ISO, and other styles

3

Mizusawa, K., K. Kikuchi, Y. Takeoka, M. Rikukawa, and K. Sanui. "Architecture and surface morphology of organic-inorganic hybrid compounds." Synthetic Metals 137, no. 1-3 (April 2003): 907–8. http://dx.doi.org/10.1016/s0379-6779(02)01025-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Kracke, Andreas, Carsten von Hänisch, and Nina Kramer. "Hybrid Cage Compounds with Organic and Inorganic Building Blocks." European Journal of Inorganic Chemistry 2012, no. 18 (May 14, 2012): 2975–79. http://dx.doi.org/10.1002/ejic.201200384.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Stock, Norbert, Christian Jargstorff, and Steffanie Wriedt. "Two New Crystalline Organogermanate-Based Inorganic-Organic Hybrid Compounds." Zeitschrift für anorganische und allgemeine Chemie 637, no. 5 (February 21, 2011): 572–77. http://dx.doi.org/10.1002/zaac.201000406.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

SUGAHARA, Yoshiyuki. "Chemical processes employing inorganic layered compounds for inorganic and inorganic^|^ndash;organic hybrid materials." Journal of the Ceramic Society of Japan 122, no. 1427 (2014): 523–29. http://dx.doi.org/10.2109/jcersj2.122.523.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Chujo, Yoshiki, and Ryo Tamaki. "New Preparation Methods for Organic–Inorganic Polymer Hybrids." MRS Bulletin 26, no. 5 (May 2001): 389–92. http://dx.doi.org/10.1557/mrs2001.92.

Full text

Abstract:

Nano-ordered composite materials consisting of organic polymers and inorganic compounds have been attracting attention for their use in creating high-performance or high-functionality polymeric materials. The term “polymer hybrid” describes blends of organic and inorganic components with molecular-level dispersions.

APA, Harvard, Vancouver, ISO, and other styles

8

Wang, Dong-Yan, Xue-Li Hou, and Xue-Nan Li. "Isostructural organic–inorganic hybrid compounds: triethylcholine tribromidocadmate and triethylcholine tribromidomercurate." Acta Crystallographica Section C Structural Chemistry 71, no. 8 (July 25, 2015): 728–32. http://dx.doi.org/10.1107/s2053229615013303.

Full text

Abstract:

In order to search for new anionic architectures and develop useful organic–inorganic hybrid materials in halometallate systems, two new crystalline organic–inorganic hybrid compounds have been prepared,i.e. catena-poly[triethyl(2-hydroxyethyl)azanium [[bromidocadmate(II)]-di-μ-bromido]], {(C8H20NO)[CdBr3]}n, (1), andcatena-poly[triethyl(2-hydroxyethyl)azanium [[bromidomercurate(II)]-di-μ-bromido]], {(C8H20NO)[HgBr3]}n, (2), and the structures determined by X-ray diffraction analysis. The compounds are isostructural, crystallizing in the space groupP21/n. The metal centres are five-coordinated by bromide anions, giving a slightly distorted trigonal–bipyramidal geometry. The crystal structures consist of one-dimensional edge-sharing chains ofMBr5trigonal bipyramids, between which triethylcholine counter-cations are intercalated. O—H...Br hydrogen-bonding interactions are present between the cations and anions.

APA, Harvard, Vancouver, ISO, and other styles

9

Fan, Le-Qing, Xin Jin, Dong-Xu Li, Chong-Bin Tian, and Ji-Huai Wu. "[Pb3Cu2I10(phen)4]n: a novel organic–inorganic hybrid ferromagnetic semiconductor." Dalton Transactions 46, no. 43 (2017): 14738–41. http://dx.doi.org/10.1039/c7dt03237d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Li, Ying, Han-Ying Li, Kai-Chi Chang, Hsiu-Mei Lin, and Chih-Min Wang. "Recent developments in organic–inorganic hybrid metal phosphates and phosphites." Dalton Transactions 50, no. 29 (2021): 10014–19. http://dx.doi.org/10.1039/d1dt01016f.

Full text

Abstract:

This frontier article highlights recent advances in synthesis and characterization of organic–inorganic hybrid metal phosphates and phosphites. The synthetic strategies and structural stabilities of hybrid composites blended with stable crystalline compounds are presented.

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Inorganic-organic hybrid compounds"

1

Bhat, Jerome C. "Electroluminescent hybrid organic/inorganic quantum dot devices." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.298766.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Reinheimer, Eric Wade. "Hybrid inorganic-organic, organic charge transfer, and radical based compounds with chalcofulvalene donors and organic acceptors." [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-2452.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Yu, Yaqin Albrecht-Schmitt Thomas E. "Studies on the structures and properties of bimetallic uranium transition metal and hybrid organic-inorganic compounds." Auburn, Ala, 2009. http://hdl.handle.net/10415/1748.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Hibino, Takashi, Atsuko Tomita, Mitsuru Sano, Toshio Kamiya, Masahiro Nagao, and Pilwon Heo. "Sn0.9In0.1P2O7-Based Organic/Inorganic Composite Membranes : Application to Intermediate-Temperature Fuel Cells." The Electrochemical Society, 2007. http://hdl.handle.net/2237/18430.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Bandara, Nilantha. "Guest intercalation into metal halide inorganic-organic layered perovskite hybrid solids and hydrothermal synthesis of tin oxide spheres." Master's thesis, Mississippi State : Mississippi State University, 2008. http://library.msstate.edu/etd/show.asp?etd=etd-10312008-212759.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

STAGI, LUIGI. "Optical and structural characterization of metal oxides and carbon nitride compounds for the development of organic/inorganic hybrid systems." Doctoral thesis, Università degli Studi di Cagliari, 2016. http://hdl.handle.net/11584/266677.

Full text

Abstract:

Metal oxides (MOs) play a key role in many areas of chemistry, physics and materials science. They are characterized by a wide variety of high technological interest compounds (e.g. TiO2, Fe3O4, Fe2O3, Y2O3, ZnO). The still increasing interest for this class of materials is mainly due to the ability to take advantage of their diversity to find new important applications in several research field. Their applicability, strengthened by the low cost, safety, ease of synthesis, ranges from (photo)catalysis to microelectronics and in vivo biological studies. Most of the MOs-based devices present outstanding performance derived from their reduced dimensions. To date, the research on nanostructured MOs is highly active in order to deeper gain knowledge about surface states and their influence on chemical and physical properties, motivating an always more multidisciplinary approach. However, some characteristics of oxides can limit their use, e.g. high band gap with almost negligible absorption in the visible, lack of optical response (luminescence) or conduction band edge not sufficiently negative to promote proton reduction (limited photocatalytic activity). The introduction of doping elements in the MO matrix to reduce these limitations can have the drawbacks of the new defects generation at the surface and/or in the bulk. Other limitations can be overcome by creating hybrid materials, such as organic and inorganic systems. In such scenario, it is necessary a detailed study aimed to characterize the properties of organic material and the means of implementation of the hybrid system. In the first part of the present thesis, we examine the stability of some exemplar metal oxides systems. The aim of this work is to extend the comprehension of nanostructured MOs phase transformation and to analyse the conditions for which the transformation takes place. The second part presents a study on carbon nitride (CN) based molecular materials performed with spectroscopy and X-ray diffraction experiments. Our characterizations reveal that CN materials present high chemical and physical stability and good control of the optical properties. Finally, we propose a structural and optical characterization of some carbon-nitride/ metal oxides hybrids. Firstly, we focus on Tb3+ doped Y2O3 system, a good candidate for nanosized phosphors, where organic passivation of the surfaces by melamine (C3H6N6) has the dual role of replacing species for hydroxides quenchers and activators of Tb by energy transfer mechanism. Then, we conclude with TiO2/CN hybrids for photocatalysis applications, realized by chemical methods and atomic layer deposition, stressing the importance of functional and terminating groups of molecular systems.

APA, Harvard, Vancouver, ISO, and other styles

7

Reis, Márcio José dos. "Síntese e caracterização de hidróxidos duplos lamelares preparados na presença de polímeros orgânicos ou com macromoléculas intercaladas." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/59/59138/tde-16062009-134859/.

Full text

Abstract:

Compostos lamelares do tipo da hidrotalcita ou hidróxidos duplos lamelares (HDL), são materiais que possuem notáveis propriedades estruturais, químicas, eletrônicas, iônicas, ópticas e magnéticas. Em função dessas propriedades, os HDL apresentam uma diversidade de aplicações tais como adsorventes e catalisadores. Este trabalho tem por objetivo utilizar polímeros e macromoléculas na preparação e caracterização de HDL, visando melhorar as propriedades texturais dos HDL de MgAl-CO3 preparados em meio contendo polímeros orgânicos ou a intercalação direta de dendrímeros tipo PAMAM de gerações -0,5 e +0,5 em HDL do sistema Zn/Al. Os HDL de MgAl-CO3 foram preparados pela adaptação do método de coprecipitação a pH decrescente, com a presença de polímeros solubilizados no meio, como molde. Os materiais foram caracterizados por difração de Raios X, análise termogravimétrica, espectroscopia no infravermelho e medidas de área superficial por BET. Baseando-se nos resultados obtidos, pode-se concluir que propriedades texturais dos HDL preparados são modificadas, quando na presença de alguns polímeros. Na maioria dos casos, os valores calculados de área superficial específica foram mais elevados, em comparação com aquele obtido para o HDL preparado em meio reacional sem polímero. Isto pode ser explicado pela diminuição do tamanho de partículas e aumento no diâmetro médio de poros dos materiais preparados, provocada pela presença de polímeros no meio reacional. Os HDL intercalados com dendrímeros PAMAM G-0,5 e PAMAM G+0,5 foram preparados por duas rotas diferentes: coprecipitação a pH constante e troca iônica em fase dupla. Os materiais obtidos foram caracterizados por meio de difração de Raios X, análise de termogravimétrica associada à espectrometria de massas e espectroscopia no infravermelho. Utilizando os dois procedimentos de preparação, a intercalação de PAMAM G-0,5 deu origem a HDL com os mesmos espaçamentos basais, concordando com a intercalação dos ânions do dendrímero em um arranjo perpendicular à lamela do HDL, enquanto que para a intercalação do PAMAM G+0,5, espaçamentos basais muito menores do que o tamanho da molécula foram obtidos. A diferença entre a distância interlamelar observada e a esperada pode ser explicada por um arranjo peculiar das moléculas desse dendrímero em uma forma elipsoidal, devido às interações intramoleculares. Espectros no infravermelho confirmam a presença dos dendrímeros nos materiais Zn2Al-PAMAM G-0,5 e Zn2Al-PAMAM G+0,5. Finalmente, a presença destes dendrímeros foi confirmada por análise térmica associada com espectrometria de massas. Os estudos de Raios X com variação de temperatura in situ e as análises termogravimétricas revelaram que o material obtido pela intercalação do PAMAM G+0,5 é termicamente menos estável do que aquele intercalado com PAMAM G-0,5, concordando com a diferença de estabilidade entre os dendrímeros livres.
Hydrotalcite-like lamellar compounds or layered double hydroxides (LDH) are materials that present notable structural, chemical, electronic, ionic, optical and magnetic properties. Depending on these properties, the LDH present a great variety of applications such as adsorbents and catalysts. The aim of this work is to prepare and to characterize MgAl-CO3-LDH prepared in aqueous media containing organic polymer to improve textural properties, and to prepare HDL by intercalation of dendrimer (PAMAM) of generations -0.5 and +0.5 in ZnAl-HDL. MgAl-CO3-HDL samples were prepared by an adaptation of the coprecipitation method at decreasing pH, with the presence of polymers in the aqueous media as template. The materials were characterized by powder X-ray diffraction, termogravimetric analysis, infrared spectroscopy and BET isotherms. Based on the obtained results, it can be concluded that the textural properties of the prepared LDH were modified. The calculated values of specific surface area were higher in most of the cases compared with those obtained by the LDH prepared without polymer due to a decrease of the particle size and an increase in the average pore diameter of the prepared materials due to the presence of polymers. HDL with intercalated (PAMAM) dendrimers G-0.5 and G+0.5 were prepared by two different methods: coprecipitation at constant pH, and ionic exchange in double phase. The obtained materials were characterized by powder X-ray diffraction, thermal gravimetric analysis associated with mass spectrometry, and infrared spectroscopy. X-ray powder diffraction patterns exhibit the characteristic profiles of the lamellar materials with basal spacing depending on the nature of the dendrimer. For both preparation methods, the intercalation of PAMAM G-0.5 gives rise to LDH with basal spacing in agreement with the dendrimer molecules perpendicular to the layer of the host structure, while for PAMAM G+0.5 a basal spacing smaller than the molecule size was obtained. The difference between the obtained and the expected value is explained by an accommodation of the dendrimer molecule in an ellipsoidal shape, due to the intra-molecular interactions. Infrared spectra confirm the presence of dendrimers in the Zn2Al-PAMAM G-0.5 and Zn2Al-PAMAM G+0.5 materials. Finally, thermal analyses associated with mass spectrometry confirm the presence of these dendrimers. Powder X-ray diffraction with in situ temperature variation reveals that the material obtained by the PAMAM G+0.5 intercalation is thermally less stable than that prepared by PAMAM G-0.5 intercalation, in agreement with the difference in the thermal stability of the free dendrimers.

APA, Harvard, Vancouver, ISO, and other styles

8

Tlatlik, Harald. "Neue Untersuchungen zu Wachstum und Struktur von Fluorapatit-Gelatine-Nanokompositen." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2009. http://nbn-resolving.de/urn:nbn:de:bsz:14-ds-1239970399481-29675.

Full text

Abstract:

Die vorliegende Dissertation beschäftigt sich mit Wachstum und Aufbau von Fluorapatit-Gelatine-Nanokompositaggregaten. Diese Aggregate werden im sogenannten Doppeldiffusionsversuch biomimetisch erzeugt und ihre äußere Form bzw. Formentwicklung lässt sich anhand eines fraktalen Modells bis ins Detail nachvollziehen. Sie zeigen einen komplexen inneren Aufbau, in dem die Makromoleküle der organischen Komponente einerseits im Zentrum jeder Nanoeinheit und andererseits zu Strängen, den sogenannten Fibrillen, zusammengelagert am Aufbau der Kompositaggregate beteiligt sind. Im Fall des Kompositkeims ist die innere Architektur in hoher Detailstufe verstanden, auch wenn -- insbesondere bezüglich der späteren Wachstumsphasen -- eine Reihe ungeklärter Fragestellungen verbleibt. Ein zentrales Ergebnis der vorliegenden Arbeit bildet die Entdeckung eines weiteren Wachstumstypen, der im Vergleich zu den bekannten, fraktalen Kompositaggregaten grundsätzliche Unterschiede bezüglich des inneren und äußeren Aufbaus zeigt. Der Grund für die andersartige Formentwicklung liegt in der Versteifung der organischen Komponente durch eine vorangegangene Einlagerung von Calciumionen, wie sowohl experimentell als auch mit atomistischen Computersimulationen gezeigt werden konnte. Aufgrund der hohen Komplexität des Systems ist es bislang allerdings nicht möglich, lokale Ionen-Konzentrationen und pH-Werte vor bzw. während Nukleation und Wachstum der Kompositaggregate im Doppeldiffusionsversuch zu bestimmen. Deshalb wurde ein Ersatzversuch -- der sehr ähnlich strukturierte Aggregate erzeugt, sich aber mit rechnerischen Methoden analysieren lässt -- entworfen und untersucht. Anhand dieser Ergebnisse konnte erstmals die "Geschichte" von Fluorapatit-Gelatine-Nanokompositaggregaten detailliert nachvollzogen werden. Da über die Rolle der Gelatine beim Wachstum der Kompositaggregate nur wenig bekannt ist, wurde eine Reihe von Versuchen durchgeführt, in denen Gelatinen mit verschiedenen Molekülmassenverteilungen eingesetzt wurden. Es stellte sich heraus, dass für selbstorganisiertes und insbesondere fraktales Wachstum der Kompositaggregate lange, möglichst wenig gestörte Makromoleküle von zentraler Wichtigkeit sind. Um die Funktion der organischen Komponente für das Kompositwachstum näher zu untersuchen, wurden Oberflächen von Kompositkeimen mit rasterkraftmikroskopischen Methoden studiert. Durch Säuberung der Oberflächen konnten Austrittsstellen der organischen Komponente durch die Oberfläche der Kompositkeime identifiziert werden. Damit konnte gezeigt werden, dass die organische Komponente aus dem Inneren des Festkörpers teilweise durch die Oberfläche dringt und somit während des Wachstums weit in das Gel hineinreichen sollte. Für die mesoskopische Strukturbildung der Kompositaggregate spielen intrinsische elektrische Felder eine essenzielle Rolle. Deshalb wurde bislang eine Wirkung externer elektrischer Felder auf das Wachstum der Kompositaggregate vermutet. Im Rahmen der vorliegenden Arbeit wurde herausgearbeitet, dass es zwar zu keiner direkten Beeinflussung kommen kann, jedoch in den elektrodennahen Bereichen des Gels eine Ordnung der organischen Moleküle durch externe elektrische Felder zu erwarten ist. Dies könnte eine Wirkung auf wachsende Kompositaggregate zeigen. Da diese Effekte auch aufgrund der elektrischen Felder um die dipolaren Kompositaggregate zu erwarten sind, könnte eine ähnliche Strukturierung der Gelatine in der Nähe der wachsenden Kompositaggregate stattfinden. Insgesamt wurden in dieser Arbeit eine Reihe grundlegender Beiträge zur Erforschung der biomimetisch erzeugten Fluorapatit-Gelatine-Nanokompositaggregate geleistet. Es konnten neue Erkenntnisse zur inneren und äußeren Architektur der Kompositaggregate, zu Mechanismen der Morphogenese und deren wichtigsten Einflussgrößen sowie zum Verständnis der chemisch-physikalischen Vorgänge auf atomarer Größenskala gewonnen werden. Als besonders fruchtbar erwies sich die Verbindung von Experimenten mit theoretischen Untersuchungen, so dass dieser Weg auch in Zukunft grundlegende Erkenntnisse bei der Erforschung der Biomineralisation verspricht und weiterhin verfolgt werden sollte.

APA, Harvard, Vancouver, ISO, and other styles

9

Kang, Jeonghee Peng Zhonghua. "Functional organic/inorganic hybrids and triphenylene-based dendritic materials." Diss., UMK access, 2007.

Find full text

Abstract:

Thesis (Ph. D.)--Dept. of Chemistry and School of Pharmacy. University of Missouri--Kansas City, 2007.
"A dissertation in chemistry and pharmaceutical science." Advisor: Zhonghua Peng. Typescript. Vita. Description based on contents viewed Apr. 22, 2008; title from "catalog record" of the print edition. Includes bibliographical references (leaves 160-176). Online version of the print edition.

APA, Harvard, Vancouver, ISO, and other styles

10

Tlatlik, Harald. "Neue Untersuchungen zu Wachstum und Struktur von Fluorapatit-Gelatine-Nanokompositen." Doctoral thesis, Technische Universität Dresden, 2008. https://tud.qucosa.de/id/qucosa%3A23601.

Full text

Abstract:

Die vorliegende Dissertation beschäftigt sich mit Wachstum und Aufbau von Fluorapatit-Gelatine-Nanokompositaggregaten. Diese Aggregate werden im sogenannten Doppeldiffusionsversuch biomimetisch erzeugt und ihre äußere Form bzw. Formentwicklung lässt sich anhand eines fraktalen Modells bis ins Detail nachvollziehen. Sie zeigen einen komplexen inneren Aufbau, in dem die Makromoleküle der organischen Komponente einerseits im Zentrum jeder Nanoeinheit und andererseits zu Strängen, den sogenannten Fibrillen, zusammengelagert am Aufbau der Kompositaggregate beteiligt sind. Im Fall des Kompositkeims ist die innere Architektur in hoher Detailstufe verstanden, auch wenn -- insbesondere bezüglich der späteren Wachstumsphasen -- eine Reihe ungeklärter Fragestellungen verbleibt. Ein zentrales Ergebnis der vorliegenden Arbeit bildet die Entdeckung eines weiteren Wachstumstypen, der im Vergleich zu den bekannten, fraktalen Kompositaggregaten grundsätzliche Unterschiede bezüglich des inneren und äußeren Aufbaus zeigt. Der Grund für die andersartige Formentwicklung liegt in der Versteifung der organischen Komponente durch eine vorangegangene Einlagerung von Calciumionen, wie sowohl experimentell als auch mit atomistischen Computersimulationen gezeigt werden konnte. Aufgrund der hohen Komplexität des Systems ist es bislang allerdings nicht möglich, lokale Ionen-Konzentrationen und pH-Werte vor bzw. während Nukleation und Wachstum der Kompositaggregate im Doppeldiffusionsversuch zu bestimmen. Deshalb wurde ein Ersatzversuch -- der sehr ähnlich strukturierte Aggregate erzeugt, sich aber mit rechnerischen Methoden analysieren lässt -- entworfen und untersucht. Anhand dieser Ergebnisse konnte erstmals die "Geschichte" von Fluorapatit-Gelatine-Nanokompositaggregaten detailliert nachvollzogen werden. Da über die Rolle der Gelatine beim Wachstum der Kompositaggregate nur wenig bekannt ist, wurde eine Reihe von Versuchen durchgeführt, in denen Gelatinen mit verschiedenen Molekülmassenverteilungen eingesetzt wurden. Es stellte sich heraus, dass für selbstorganisiertes und insbesondere fraktales Wachstum der Kompositaggregate lange, möglichst wenig gestörte Makromoleküle von zentraler Wichtigkeit sind. Um die Funktion der organischen Komponente für das Kompositwachstum näher zu untersuchen, wurden Oberflächen von Kompositkeimen mit rasterkraftmikroskopischen Methoden studiert. Durch Säuberung der Oberflächen konnten Austrittsstellen der organischen Komponente durch die Oberfläche der Kompositkeime identifiziert werden. Damit konnte gezeigt werden, dass die organische Komponente aus dem Inneren des Festkörpers teilweise durch die Oberfläche dringt und somit während des Wachstums weit in das Gel hineinreichen sollte. Für die mesoskopische Strukturbildung der Kompositaggregate spielen intrinsische elektrische Felder eine essenzielle Rolle. Deshalb wurde bislang eine Wirkung externer elektrischer Felder auf das Wachstum der Kompositaggregate vermutet. Im Rahmen der vorliegenden Arbeit wurde herausgearbeitet, dass es zwar zu keiner direkten Beeinflussung kommen kann, jedoch in den elektrodennahen Bereichen des Gels eine Ordnung der organischen Moleküle durch externe elektrische Felder zu erwarten ist. Dies könnte eine Wirkung auf wachsende Kompositaggregate zeigen. Da diese Effekte auch aufgrund der elektrischen Felder um die dipolaren Kompositaggregate zu erwarten sind, könnte eine ähnliche Strukturierung der Gelatine in der Nähe der wachsenden Kompositaggregate stattfinden. Insgesamt wurden in dieser Arbeit eine Reihe grundlegender Beiträge zur Erforschung der biomimetisch erzeugten Fluorapatit-Gelatine-Nanokompositaggregate geleistet. Es konnten neue Erkenntnisse zur inneren und äußeren Architektur der Kompositaggregate, zu Mechanismen der Morphogenese und deren wichtigsten Einflussgrößen sowie zum Verständnis der chemisch-physikalischen Vorgänge auf atomarer Größenskala gewonnen werden. Als besonders fruchtbar erwies sich die Verbindung von Experimenten mit theoretischen Untersuchungen, so dass dieser Weg auch in Zukunft grundlegende Erkenntnisse bei der Erforschung der Biomineralisation verspricht und weiterhin verfolgt werden sollte.

APA, Harvard, Vancouver, ISO, and other styles

More sources

Books on the topic "Inorganic-organic hybrid compounds"

1

1934-, Mark James E., Lee C. Y.-C. 1947-, Biancini P. A. 1957-, and American Chemical Society. Division of Polymeric Materials: Science and Engineering., eds. Hybrid organic-inorganic composites. Washington, D.C: American Chemical Society, 1995.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

2

C, Klein Lisa, ed. Organic/inorganic hybrid materials II. Warrendale, Penn: Materials Research Society, 1999.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

3

1954-, Nalwa Hari Singh, ed. Handbook of organic-inorganic hybrid materials and nanocomposites. Stevenson Ranch, Calif: American Scientific Publishers, 2003.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

4

Taubert, Andreas, and Marie Helene Delville. Hybrid Organic-Inorganic Interfaces: Towards Advanced Functional Materials. Wiley & Sons, Incorporated, John, 2017.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

5

Taubert, Andreas, and Marie Helene Delville. Hybrid Organic-Inorganic Interfaces: Towards Advanced Functional Materials. Wiley & Sons, Incorporated, John, 2017.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

6

Taubert, Andreas, and Marie Helene Delville. Hybrid Organic-Inorganic Interfaces: Towards Advanced Functional Materials. Wiley & Sons, Incorporated, John, 2017.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

7

Taubert, Andreas, and Marie Helene Delville. Hybrid Organic-Inorganic Interfaces: Towards Advanced Functional Materials. Wiley & Sons, Limited, John, 2017.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

8

Taubert, Andreas, and Marie Helene Delville. Hybrid Organic-Inorganic Interfaces: Towards Advanced Functional Materials. Wiley & Sons, Limited, John, 2018.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

9

Klein, Lisa C., James E. Mark, Lorraine F. Francis, and Mark R. De Guire. Organic/Inorganic Hybrid Materials II: Volume 576. University of Cambridge ESOL Examinations, 2014.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

10

(Editor), J. E. Mark, C. C.-Y. Lee (Editor), and P. A. Bianconi (Editor), eds. Hybrid Organic-Inorganic Composites (Acs Symposium Series). An American Chemical Society Publication, 1998.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Book chapters on the topic "Inorganic-organic hybrid compounds"

1

Rabu, Pierre, Marc Drillon, Kunio Awaga, Wataru Fujita, and Taketoshi Sekine. "Hybrid Organic-Inorganic Multilayer Compounds: Towards Controllable and/or Switchable Magnets." In Magnetism: Molecules to Materials, 357–95. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2003. http://dx.doi.org/10.1002/9783527620548.ch11a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Li, Jing, and Ruibo Zhang. "A New Class of Nanostructured Inorganic-Organic Hybrid Semiconductors Based on II-VI Binary Compounds." In Progress in Inorganic Chemistry, 445–504. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118148235.ch8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Papavassiliou, George C., George A. Mousdis, and Ioannis B. Koutselas. "Excitonic Bands in the Spectra of Some Organic-Inorganic Hybrid Compounds Based on Metal Halide Units." In Molecular Materials and Functional Polymers, 113–19. Vienna: Springer Vienna, 2001. http://dx.doi.org/10.1007/978-3-7091-6276-7_11.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Tulis, A. J. "Powerful Insensitive Hybrid Explosives Using Inorganic Propellants/Pyrotechnics in Conjunction with Organic CHO Compounds for Tailorable Blast Applications." In Application of Demilitarized Gun and Rocket Propellants in Commercial Explosives, 215–32. Dordrecht: Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4381-3_27.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Kandare, Everson, Daniel Hall, David D. Jiang, and Jeanne M. Hossenlopp. "Development of New Fire Retardant Additives Based on Hybrid Inorganic-Organic Nanodimensional Layered Compounds: Thermal Degradation of PMMA Composites." In ACS Symposium Series, 131–43. Washington, DC: American Chemical Society, 2005. http://dx.doi.org/10.1021/bk-2006-0922.ch011.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Bauer, S., and N. Stock. "High-throughput strategies for the solvothermal synthesis of inorganic-organic hybrid compounds." In From Zeolites to Porous MOF Materials - The 40th Anniversary of International Zeolite Conference, Proceedings of the 15th International Zeolite Conference, 2015–20. Elsevier, 2007. http://dx.doi.org/10.1016/s0167-2991(07)81093-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Nawaz Shariff, Shakeel, Supriya Saravu, and Dileep Ramakrishna. "Schiff Base Complexes for Catalytic Application." In Schiff Base in Organic, Inorganic and Physical Chemistry [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.107904.

Full text

Abstract:

Primary amines are combined with an aldehyde group to generate Schiff base compounds, which are called condensation imine products. This class of compounds has a general structure, R-C=NR\', where R and R\' represent alkyl/aryl/cyclohexyl/heterocyclic group. These compounds contain an azomethine group that is basic in nature due to, (i) the presence of lone pair of electrons on the nitrogen and (ii) electron-donating nature of the double bond. Hence, these compounds, as ligands, participate in the formation of metal complexes. The presence of lone pair of electrons on the nitrogen atom and the hybridization involved explains the physical, chemical, and spectral properties of nitrogen-containing moieties. In the case of (sp2) hybridization (trigonal structure), the lone pair of electrons occupies either a symmetrical unhybridized 2p orbital that is perpendicular to the plane of trigonal hybrids or a symmetrical hybrid orbital, whose axis is in the plane, leaving behind only the π-electrons in the unhybridized 2p orbital. A very similar type of hybridization is experienced by the nitrogen atom in the azomethine group. Traditional phosphine complexes of nickel, palladium, and platinum, particularly those of palladium, have played an extremely important role in the development of homogeneous catalysis. Schiff base complexes as catalysts have been studied for various organic transformations such as oxidation, epoxidation, reduction, coupling reactions, polymerization reactions, hydroformylations, and many more.

APA, Harvard, Vancouver, ISO, and other styles

8

Silva, Cecilia Santos, Nattany Tayany Gomes De Paula, Severino Alves, and Ana Paula Silveira Paim. "Application of Metal–Organic Framework Nanocomposites." In Metal–Organic Frameworks in Analytical Chemistry, 415–53. The Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781839167485-00415.

Full text

Abstract:

Metal–organic frameworks (MOFs) are now being considered as the most promising materials within the class of coordination polymers. In recent years, many studies have presented MOFs as a class of organic–inorganic hybrid compounds that can be used as supports for the development of multifunctional materials. Nanocomposites have been receiving increasing attention due to the simplicity and versatility of the synthetic approach as well as the incorporation of properties of the single components and synergistic relations, achieving a vast area of science and technology The applications of MOF nanocomposites such as biological applications, sensing, adsorption, catalysis and extraction have been presented in this chapter. We have highlighted some already-studied applications and discussed the advantages and disadvantages of using MOF nanocomposites compared to other conventional or less traditional procedures, emphasizing the properties that influence their potential applications.

APA, Harvard, Vancouver, ISO, and other styles

9

Chen, Deliang. "Topochemical Conversion of Inorganic–Organic Hybrid Compounds into Low-Dimensional Inorganic Nanostructures with Smart Control in Crystal-Sizes and Shapes." In Crystallization and Materials Science of Modern Artificial and Natural Crystals. InTech, 2012. http://dx.doi.org/10.5772/28418.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Vaidhyanathan, R., Srinivasan Natarajan, and C. N. R. Rao. "Hybrid Inorganic–Organic Host–Guest Compounds: Open-Framework Cadmium Oxalates Incorporating Novel Extended Structures of Alkali Halides." In World Scientific Series in 20th Century Chemistry, 522–31. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812835734_0069.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Inorganic-organic hybrid compounds"

1

Dantal, B. R., S. Gupta, A. Saigal, M. A. Zimmerman, and I. Georgakoudi. "Characterization of a New Titanium Dioxide-Polymer Nanocomposite Material for Electronic Packaging Using Light Scattering Spectroscopy." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-69194.

Full text

Abstract:

During the last decade there has been a great progress in the field of inorganic and organic hybrid material development and characterization techniques. Mechanical, optical and electrical properties of these hybrid materials heavily depend upon the percentage composition of inorganic and organic components of these hybrid materials [1–3]. Generally, inorganic particle distribution in the organic polymer is characterized using Scanning Electron Microscopy. In this paper we introduce an optics based technique for composite materials characterization. In our research, Titania pigments are used in molding compounds to improve opacity by increasing scattering efficiency of the medium. The light scattering efficiency of the samples is found to be increasing with the addition of Titania particles in the base polymer. This systematic increase of light scattering is attributed to the surface morphology, variation of refractive index due to addition of Titania particles.

APA, Harvard, Vancouver, ISO, and other styles

2

Lekishvili, N., Kh Barbakadze, W. Brostow, T. Datashvili, A. Fainleib, and O. Grigorieva. "Inorganic-organic hybrid antibiocorrosive covers based on polyurethanes and coordination compounds of some transition metals." In 6TH INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2012. http://dx.doi.org/10.1063/1.4738469.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

PAPAVASSILIOU, G. C., G. A. MOUSDIS, I. B. KOUTSELAS, and G. J. PAPAIOANNOU. "EXCITONIC BANDS IN THE PHOTOCONDUCTIVITY SPECTRA OF SOME ORGANIC-INORGANIC HYBRID COMPOUNDS BASED ON METAL HALIDE UNITS." In Proceedings of 2000 International Conference. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811387_0036.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Duartey, K. O., A. K. Quainoo, and C. K. Darko. "Evaluation Studies of KCl and Amino Acid Mixtures for Clay Stabilization and Rheological Enhancement of Water-Based Fracturing Fluids." In SPE Nigeria Annual International Conference and Exhibition. SPE, 2023. http://dx.doi.org/10.2118/217118-ms.

Full text

Abstract:

Summary Conventional stabilizers such as inorganic salts in water-based fluids are restricted for use in gas and oil shales drilling and hydraulic fracturing for drilling due to environmental, economic and performance concerns. For example, 2% use of KCl, a commonly used inorganic salt, contains an excess of 9500ppm chloride. This is considered high and toxic. Apart from environmental problems, KCl inhibiting solutions tend to negatively affect the rheology of the water-based fluids, posing a dilemma for industry operators. The clay and rheological stabilizing effects of KCl and amino acid mixes for hydraulic fracturing operations were investigated in this study. The stabilizing and rheological potentials of mixes of KCl and organic compounds have proven to be superior to the separate compounds in studies. The KCl was used in the study at safe quantities (1%) to prevent toxicity concerns. In this study, the inhibition potentials of KCl+ Arginine and KCl + Alanine solutions, mixed approximately at ecologically safe quantities, were tested at different bentonite wafers using M4600 Linear swell at 25°C and 1000psi in the work. Furthermore, rheological studies on bentonite-based suspensions were carried out using a high-precision Discovery Hybrid Rheometer (DHR-1). This was done to monitor the flow parameters of the inhibiting suspensions and their anti-swelling effects on the bentonite component of the prepared fracturing fluid. The effects of the mixtures were also compared to that of KCl, Arginine and Alanine inhibition solutions. Herschel-Bulkley's model was also used to determine the flow characteristics. After 24 hours of testing, the swelling findings reveal that KCl+ Arginine/KCl + Alanine treated fracturing fluids significantly affect the clay stabilization and rheological properties of the fracturing fluid. The study provides basic information on the inhibition potentials of KCl and natural amino acid mixtures in water-based fracturing fluids for clean clay stabilization.

APA, Harvard, Vancouver, ISO, and other styles

5

Kelkar, Rohit, Satwik Timmavajjala, Kunal Mitra, and Clayton Baum. "Fabrication and Characterization of Hybrid Nano-Polymer Solar Cells." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-65546.

Full text

Abstract:

Hybrid solar cells consist of organic as well as inorganic substances. An organic compound absorbs light and transports holes whereas an inorganic compound is an acceptor and transports electrons. Hybrid solar cells were fabricated on glass slides pre-coated with indium tin oxide (ITO) which itself acts as a cathode. Poly(3,4 ethylenedioxythiophene)polystyrenesulfonate (PEDOT:PSS) was coated in order to avoid a short circuit between the layers and also to smooth the surface of ITO. A photoactive layer which consisted of poly(3-hexathiophene) (P3HT), TiO2 and star dispersant was coated over the PEDOT:PSS layer. Gold/molybdenum was sputtered as an anode material. Star dispersant was added to the active layer in order to improve the performance of the solar cell. Introduction of star dispersant increases the interfacial area and in turn the exciton dissociation. Atomic force microscopy (AFM) was used to measure the thicknesses of the individual layers and also to obtain a topographical view of the cell surface to ensure the uniformity of the deposited layers. Absorption and photoluminescence spectra were measured to characterize the solar cell. Finally, current–voltage characteristics were measured to ensure that the solar cell acts as a diode.

APA, Harvard, Vancouver, ISO, and other styles

6

Wu, Qiong, XiangQing Zhu, Hai Yang, He Ping, Jinglong Luo, Zheng Ying, Hai Wang, QuanShui Fan, and EnBo Wang. "Metal-salen derivatives of polyoxometalates crystalline material: A new inorganic-organic hybrid compound exhibiting photocatalytic properties." In 2013 International Conference on Materials for Renewable Energy and Environment (ICMREE). IEEE, 2013. http://dx.doi.org/10.1109/icmree.2013.6893753.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!