Log in

Relevant bibliographies by topics / Supramolecular organometallic chemistry

Contents

Journal articles
Dissertations / Theses
Books
Book chapters

Academic literature on the topic 'Supramolecular organometallic chemistry'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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 'Supramolecular organometallic chemistry.'

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 "Supramolecular organometallic chemistry"

1

Severin, Kay. "Supramolecular chemistry with organometallic half-sandwich complexes." Chemical Communications, no. 37 (2006): 3859. http://dx.doi.org/10.1039/b606632c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Yeung, Margaret Ching-Lam, and Vivian Wing-Wah Yam. "Luminescent cation sensors: from host–guest chemistry, supramolecular chemistry to reaction-based mechanisms." Chemical Society Reviews 44, no. 13 (2015): 4192–202. http://dx.doi.org/10.1039/c4cs00391h.

Full text

Abstract:

This highlight provides a brief overview on luminescent cation detection strategies derived from a wide variety of organic and organometallic architectures, including those based on the ion-receptor complementarity, integrated with the extension of the concept of supramolecular chemistry and those using the irreversible analyte-specific reactions.

APA, Harvard, Vancouver, ISO, and other styles

3

Atencio, Reinaldo, Lee Brammer, Shiyue Fang, and F. Christopher Pigge. "π-Bonded organometallic building blocks for supramolecular chemistry." New Journal of Chemistry 23, no. 5 (1999): 461–63. http://dx.doi.org/10.1039/a901925a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Bhowmick, Sourav, Sourav Chakraborty, Atanu Das, P. R. Rajamohanan, and Neeladri Das. "Pyrazine-Based Organometallic Complex: Synthesis, Characterization, and Supramolecular Chemistry." Inorganic Chemistry 54, no. 6 (February 26, 2015): 2543–50. http://dx.doi.org/10.1021/ic502581x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Schindler, Andrea, Claudia Heindl, Gábor Balázs, Christian Gröger, Alexander V. Virovets, Eugenia V. Peresypkina, and Manfred Scheer. "Size-Determining Dependencies in Supramolecular Organometallic Host-Guest Chemistry." Chemistry - A European Journal 18, no. 3 (December 13, 2011): 829–35. http://dx.doi.org/10.1002/chem.201103141.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Laskoski, Matthew, Jason G. M. Morton, Mark D. Smith, and Uwe H. F. Bunz. "A supramolecular organometallic–metalorganic square." Chem. Commun., no. 14 (2003): 1628–29. http://dx.doi.org/10.1039/b304169g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Ma, Li-Li, Jia-Qin Han, Wei-Guo Jia, and Ying-Feng Han. "Coordination-driven self-assembly vs dynamic covalent chemistry: versatile methods for the synthesis of molecular metallarectangles." Beilstein Journal of Organic Chemistry 14 (August 3, 2018): 2027–34. http://dx.doi.org/10.3762/bjoc.14.178.

Full text

Abstract:

Supramolecular coordination assemblies have a range of potential applications in chemical and biological sciences. Herein, simple modular methods for the synthesis of metallarectangles are described. The desired tetranuclear metallarectangles were synthesized by using coordination-driven self-assembly of half-sandwich rhodium-based organometallic clip units and organic ligands. The reaction of such an organometallic clip with 4-formylpyridine provided a dinuclear molecular tweezer with pendant aldehyde groups, and subsequent [4 + 4] condensation reactions with diamines provides another route to the target metallarectangles in good yields. The same assemblies can also be easily isolated in one-pot procedures by mixing the organometallic clip, diamines and 4-formylpyridine.

APA, Harvard, Vancouver, ISO, and other styles

8

Aguiló, Elisabet, Mariona Dalmases, Mengxi Lin, João Carlos Lima, Raquel Gavara, Albert Figuerola, Jordi Llorca, and Laura Rodríguez. "Facile morphology control of gold(0) structures from aurophilic assemblies." Dalton Transactions 49, no. 14 (2020): 4200–4205. http://dx.doi.org/10.1039/d0dt00277a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Ibáñez, Susana, Macarena Poyatos, and Eduardo Peris. "N-Heterocyclic Carbenes: A Door Open to Supramolecular Organometallic Chemistry." Accounts of Chemical Research 53, no. 7 (July 9, 2020): 1401–13. http://dx.doi.org/10.1021/acs.accounts.0c00312.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Andrews, Philip C., and Colin L. Raston. "Future prospects in organometallic chemisty of the Main Group metals: small molecules — supramolecular chemistry." Journal of Organometallic Chemistry 600, no. 1-2 (April 2000): 174–85. http://dx.doi.org/10.1016/s0022-328x(00)00081-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Supramolecular organometallic chemistry"

1

Meng, Wenjing. "Metal-organic polyhedra : subcomponent self-assembly, structural properties, host-guest behavior and system chemistry." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610719.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Coombes, Matthew. "A Comparative study of two copper(II) based metal-organic frameworks : Cu2¼(OH)½B4C•8H2O and Cu2Na(OH)B4C•7H2O." Thesis, Rhodes University, 2013. http://hdl.handle.net/10962/d1016245.

Full text

Abstract:

This study focussed on two copper(II)-containing metal-organic frameworks (MOFs): Cu2Na(OH)B4C•7H2O and Cu2¼(OH)½B4C•8H2O (B4C = 1,2,4,5- benzenetetracarboxylate). They are both covalent, three-dimensional metalorganic framework polymers containing voids filled with water molecules. Both were characterised by elemental analysis, infrared spectroscopy, X-ray powder diffractometry (both in situ and regular), thermogravimetric analysis, differential scanning calorimetry and X-ray photoelectron spectroscopy. These two MOFs are essentially identical, with the only difference being the substitution of sodium by copper at every 4th site (disordered throughout the crystal). The guest inclusion properties of both MOFs were studied and compared. Although both structures collapse on dehydration, it was observed that Cu2Na(OH)B4C•7H2O is able to take up signifcant amounts of water, methanol and ethanol. All these processes are fully reversible. Car-Parrinello molecular dynamics studies suggest that it is a strong interaction between the oxygen atoms on these molecules with the sodium cation of the MOF that is responsible for this signifcant uptake. In contrast, Cu2¼ (OH)½ B4C•8H2O, the MOF without a sodium cation, did not demonstrate any methanol or ethanol uptake, but was able to take up some water. The uptake of water, however, is not a fully reversible process. The absence of sodium likely results in insuffcient energy to draw methanol and ethanol into the framework, while a subtle rotation of a carboxylate group on dehydration decreases the ability of the framework to form hydrogen bonds, thus reducing the ability to take up water. A series of hydrothermal syntheses were performed in order to develop a method of synthesis superior to the current gel-based synthesis that requires several months and has poor yields. The hydrothermal products were characterized by elemental analysis, infrared spectroscopy, X-ray powder diffractometry, thermogravimetric analysis and differential scanning calorimetry. It was shown that the MOF Cu2Na(OH)B4C•7H2O may be synthesised in almost 100% yield by using a temperature of 120°C over a period of 72 hours. It was not possible to synthesise Cu2¼ (OH)½ B4C•8H2O in a 100% yield - it was only obtained as a minor product.

APA, Harvard, Vancouver, ISO, and other styles

3

Faustino, Brissos Rosa Maria. "Coordination, organometallic and supramolecular chemistry approaches to the design of metal-based cytotoxic agents." Doctoral thesis, Universitat de Barcelona, 2018. http://hdl.handle.net/10803/544129.

Full text

Abstract:

The discovery of cisplatin and its successful use as chemotherapeutic agent have encouraged the development of metal-based anticancer molecules. The present doctoral research project includes three different chemistry approaches to design new metal-based cytotoxic compounds. Coordination, organometallic and supramolecular chemistry have been used to successfully develop three families of compounds with highly promising biological properties. Copper(II) coordination compounds of various nuclearities have been prepared from new Schiff-base ligands. The complexes strongly interact with DNA without cleaving it and exhibit notable cytotoxicities against various murine and human cancer cell lines. Organometallic ruthenium(II)-arene compounds containing a monophosphane PR3 ligand have been obtained, which show remarkable cytotoxicites against a wide panel of human cancer cells, so as very interesting antimetastatic properties. Structureactivity relationship studies have been carried out, which illustrated the great potential (and versatility) of this family of molecules, whose biological properties can be finetuned by the selection of the different ligands bound to the metal. A new family of supramolecular compounds has been developed with the objective to target the DNA major groove or/and stabilize non-conventional DNA structures, for instance the three-way junction (3WJ). The series of iron(III) metallohelicates prepared exhibit groove-binding properties but are not capable of stabilizing the 3WJ. Some of these helical complexes show interesting cytotoxic properties and one of them can even induce cell apoptosis.
El descobriment que cisplatí és un fàrmac molt útil en quimioteràpia ha encoratjat el desenvolupament de fàrmacs antitumorals basats en metalls. El projecte de recerca d’aquesta Tesi Doctoral inclou tres aproximacions diferents pel disseny de nous compostos citotòxics basats en metalls. Així doncs, tant la química de coordinació com l’organometàl·lica i supramolecular s’han emprat per desenvolupar tres famílies de compostos amb propietats biològiques molt prometedores. S’han preparat complexos de Cu(II) amb imines (bases de Shiff) de diverses nuclearitats. S’ha trobat que els complexos interaccionen fortament amb l’ADN sense escindir-lo i tenen citotoxicitats elevades en diverses línies de cèl·lules canceroses de ratolí i també humanes. S’han estudiat també compostos organometàl·lics de Ru(II) amb fosfines terciàries PR3 i s’ha trobat que són molt citotòxics en un ampli espectre de línies cel·lulars canceroses humanes. A més, presententen un efecte antimetastàtic molt interessant. S’han establert relacions estructura-propietat, fet que il·lustra el gran potencial i versatilitat d’aquesta família de molècules perquè les propietats es poden modular segons el lligand fosfina unit al metall. Finalment, s’ha desenvolupat una nova família de compostos supramoleculars amb l’objectiu que interaccionin amb el solc gran de l’ADN i/o estabilitzar estructures no convencionals de l’ADN com per exemple unions triples (3WJ). Així doncs, s’ha trobat que els metal·lohelicats de Fe(III) que s’han preparat s’uneixen al solc major de l’ADN però no son capaços d’estabilitzar les unions triples 3WJ. Alguns d’aquests compostos presenten propietats citotòxiques interessants i un d’ells fins i tot indueix l’apoptosi cel·lular.

APA, Harvard, Vancouver, ISO, and other styles

4

Cordes, David B., and n/a. "Supramolecular transition metal architectures." University of Otago. Chemistry Department, 2005. http://adt.otago.ac.nz./public/adt-NZDU20060705.144929.

Full text

Abstract:

This thesis describes the investigation of the coordination and supramolecular chemistry of three different types of pyridine-containing ligand with a selection of Ag(I), Cu(I), Cu(II) and Cd(II) salts. The ligand types are flexible and four-armed, rigid and four-armed and bent with two rigid arms. All the ligands also display the ability to form additional supramolecular interactions. Chapter one introduces supramolecular chemistry and crystal engineering and covers background on several areas of current interest in these fields. Network structures, both coordination polymers and hydrogen-bonded systems, are discussed and topological analysis as a method of describing and comparing network structures is introduced. An outline of the ligand design, choice of transition metals and anions is given. Chapter two provides a review of flexible four-armed pyridine-containing ligands and their use in coordination chemistry. The synthesis and characterisation of three flexible four-armed ligands 1,2,4,5-tetrakis(2-pyridylmethyl-sulfanylmethyl)benzene (2tet), 1,2,4,5-tetrakis(3-pyridylmethyl-sulfanylmethyl)benzene (3tet) and 1,2,4,5-tetrakis(4-pyridylmethyl-sulfanylmethyl)benzene (4tet) are given. The synthesis and characterisation of the Ag(I), Cu(II) and Cd(II) complexes formed with these three ligands are also given. The complex of [Cd(2tet)(NO₃)₄] was structurally characterised by X-ray diffraction and was found to be a discrete species. The complexes {[Ag₂(3tet)](ClO₄)₂}n̲, {[Ag₂(3tet)](PF₆)₂}n̲, {[Ag₂(3tet)](CF₃CO₂)₂}n̲, {[Ag₂(4tet)]-(ClO₄)₂�2MeCN�2CHCl₃}n̲, {[Ag₂(4tet)](PF₆)₂�6MeCN}n̲ and {[Ag₂(4tet)](ClO₄)₂-�3H₂O}n̲ were likewise structurally characterised by X-ray diffraction. All these complexes were three-dimensional coordination polymers. A comparison of the seven structures is given at the end of the chapter. Chapter three reviews rigid four-armed pyridine-containing ligands and their use in coordination chemistry. The preparation of the rigid four-armed ligand 2,3,4,5-tetrakis(4-pyridyl)thiophene (pyth) is given. The synthesis and characterisation of the Ag(I), Cu(I) and Cd(II) complexes formed with this ligand are also given. The complexes [Ag(pyth)](BF₄)�3MeCN�CH₂Cl₂}n̲, [Ag(pyth)](PF₆)�MeCN�CH₂Cl₂}n̲, [Ag(pyth)]-(CF₃SO₃)�2MeCN�CH₂Cl₂}n̲, [Cu(pyth)](PF₆)�MeCN�CH₂Cl₂}n̲ and [(Cu₂I₂)(pyth)]-(BF₄)�1/2CH₂Cl₂�H₂O}n̲ were structurally characterised by X-ray diffraction. The complex with CuI was a two-dimensional coordination polymer, and the other four complexes were three-dimensional coordination polymers. A comparison of the five structures is given at the end of the chapter. Chapter four begins with a review of rigid angular bridging ligands and their use in coordination and supramolecular chemistry. The preparation of the ligand bis(4-pyridyl)amine (bpa) is given. The structural arrangement of bpa in the solid state was determined by X-ray diffraction. Complexes of Ag(I), Cu(I), Cu(II) and Cd(II) formed with this ligand were synthesised and characterised. The complexes {[Ag(bpa)(MeCN)](CF₃SO₃)}n̲, {[Ag(bpa)](PF₆)�MeCN}n̲, {[Ag(bpa)](ClO₄)-�2MeCN}n̲, {[Ag(bpa)](ClO₄)}n̲, {[Ag(bpa)](NO₃)}n̲, [(Cu₂I₂)(bpa)₂]n̲, {[Cu(bpa)₂Cl₂]-�3DMF�3/2H₂O}n̲, {[Cd(bpa)₂(NO₃)(H₂O)](NO₃)}n̲, {[Cd(bpa)₂(SO₄)(H₂O)]�3H₂O}n̲, [Cd(bpaH)₂(SO₄)₂(H₂O)₂]�2MeCN and {[Cd(bpa)(SCN)₂]�1/5iPrOH}n̲ were structurally characterised by X-ray diffraction. All complexes with Ag(I) were one-dimensional coordination polymers, with two of them helical, the other three zigzag. Both complexes with Cu(I) and (II) were two-dimensional coordination polymers. One complex with CdSO₄ was discrete, with the bpa ligands mono-protonated, but all other three other Cd(II) complexes were three-dimensional coordination polymers. Seven of these complexes showed hydrogen-bonding interactions linking them together to form supramolecular structures of higher dimensionalities. A comparison of the twelve structures is given at the end of the chapter. Chapter five is a brief summary of the outcomes of this thesis.

APA, Harvard, Vancouver, ISO, and other styles

5

Malic, Nino 1974. "5,7,12,14-tetramethyldibenzo[b,i]-1,4,8,11-tetraazacyclotetradecine-nickel(II)ester derivatives and supramolecular complexes with ionic substrates /." Monash University, Dept. of Chemistry, 2002. http://arrow.monash.edu.au/hdl/1959.1/8331.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Martínez, Agramunt Víctor. "Nickel and palladium supramolecular organometallic complexes based on NHC-ligands with polyaromatic moieties for host-guest chemistry studies." Doctoral thesis, Universitat Jaume I, 2020. http://dx.doi.org/10.6035/14104.2020.366143.

Full text

Abstract:

Se ha obtenido una nueva familia de cuatro Complejos Organometálicos Supramoleculares (SOCs) basados en pireno. Dentro de los cuales se ha desarrollado un nuevo receptor de PAH, capaz de discernir entre los diferentes PAH en función de su forma, tamaño, y número de electrones-pi. Hemos desarrollado una estrategia eficiente para la extracción de PAH, que son compuestos tóxicos y carcinogénicos, en disolventes orgánicos. Paralelamente, se han obtenido dos receptores de fulereno, capaces de adaptar su tamaño a la forma del fulereno. Debido a la mayor afinidad respecto a un fulereno específico, mostramos un potencial nuevo método de purificación de fulerenos. Describimos el primer sistema host-guest utilizado como fotosensibilidazor en la generación de oxígeno singlete. Este SOC con fulereno atrapado, fue capaz de oxidar una gran variedad de alquenos utilizando el oxígeno singlete generado a partir de aire a presión atmosférica y luz visible. Finalmente se encapsularon multiples guests.
Three nickel-based and one palladium-based supramolecular organometallic cages have been prepared. These four cages are based on a N-heterocyclic carbene ligand with a pyrene tag, that has been key in the subsequent applications of the cage together with the inner cavity. By pi-stacking interactions, it has been possible to encapsulate both polycylic aromatic hydrocarbons and fullerenes. The interest on first group of compounds is based on their accurate toxicity while the fullerenes are interesting due to their added value. It was possible to extract the first group of molecules from an organic media through the encapsulation inside the supramolecular cages. The host-guest adduct formed with fullerenes encapsulated inside the palladium cage was used as photocatalyst of aromatic, cyclic and acyclic substrates via singlet oxygen generation. The same palladium cage was used as receptor for multiple stacks of polyaromatic compounds.
Programa de Doctorat en Ciències

APA, Harvard, Vancouver, ISO, and other styles

7

Pally, Nitin Kumar. "Synthesis and Structures of New Three-Dimensional Copper Metal-Organic Frameworks." TopSCHOLAR®, 2013. http://digitalcommons.wku.edu/theses/1295.

Full text

Abstract:

Metal-organic frameworks (MOFs) are crystalline materials with metal ions covalently bonded to organic ligands. The ligands act as spacers often creating a porous structure with very high pore volume and surface area. MOFs are known for their robust structures, high porosity, and different chemical functionalities and are considered for applications in adsorptions, separations, catalysis and gas storage. This work focuses on the synthesis of new MOFs using copper compounds. Different types of carboxylate ligands were used for the synthesis. Two new copper-organic frameworks, [Cu3(pyz)(btc)] (1), and [(Cu3(btc))•xH2O] (2) (btc= benzene-1,3,5-tricarboxylate, pyz= pyrazine) have been synthesized using hydro/solvothermal methods and have been characterized using X-ray diffraction, IR, TGA, fluorescence and CHN analysis.

APA, Harvard, Vancouver, ISO, and other styles

8

Guo, Jianping. "Synthesis, structure and characterization of long distance electrostatic force and hydrogen bond supramolecular polymers synthesis, structure and characterization of bis[2,4-di(pyridyl)-1,3,5-triazapenta-dienato] metal complexes." HKBU Institutional Repository, 2004. http://repository.hkbu.edu.hk/etd_ra/506.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Lewis, William. "Chiral Heterocyclic Ligands." Thesis, University of Canterbury. Chemistry, 2007. http://hdl.handle.net/10092/1383.

Full text

Abstract:

This thesis describes the preparation and characterisation of a number of homochiral coordination and metallosupramolecular assemblies. These species were formed from the reaction of chiral pyridine and quinoline containing ligands and metal ions. The combination of traditional coordination chemistry and supramolecular interactions led to a range of polymeric and network structures being formed. The ligands used in this thesis can be divided into two broad categories: alkaloids and ligands derived from them, and amino acid-based ligands. In the first category three new ligands were synthesized, and a variety of routes towards alkaloid-based homochiral ligands were investigated. The second category focused on three ligand motifs, and resulted in the preparation of 16 ligands. These two categories of ligands were reacted with a range of metal salts to investigate their coordination and supramolecular chemistry. The structure of twenty complexes was determined by single crystal X-ray crystallography. The complexes had a range of structures, with discrete and polymeric species being formed. Hydrogen bonding was an important feature in the supramolecular chemistry of the complexes, playing a different role in different series of complexes. Two chiral coordination polymers and one chiral coordination network were synthesized. All three of these structures possessed directionality to some degree: in the coordination network and one of the polymers the directionality is counterbalanced by the opposite directionality being present in the crystal, while the second coordination polymer is generated by the screw axis present and has a high degree of overall directionality.

APA, Harvard, Vancouver, ISO, and other styles

10

Toyama, Marcos Makoto. "Contribuição à química supramolecular de 3,4-tetra(piridil) porfirazinas tetrarutenadas." Universidade de São Paulo, 2003. http://www.teses.usp.br/teses/disponiveis/46/46134/tde-05032018-171800/.

Full text

Abstract:

Neste trabalho, descreve-se a síntese, caracterização e propriedades dos complexos derivados da tetra(3,4-piridil)porfirazina com os grupos [Ru(bipy)2Cl]1+. A conjugação eletrônica entre o resíduo piridínico e o anel da porfirazina promovem uma eficiente comunicação entre os grupos periféricos e o central, que é refletido no espectro de emissão e seu correspondente perfil de excitação. Esse tipo de comportamento revela um efeito antena no sistema H2TPyPzTRu, contrastante com as propriedades fotofisicas das porfirinas análogas TPyPRu, onde os grupos piridínicos exibem baixa interação eletrônica ao anel porfirínico. Apesar do forte acoplamento eletrônico entre os grupos perféricos e o central, as propriedades eletrônicas dos complexos de rutênio foram preservadas, exibindo potenciais redox muito próximos dos complexos livres e comportamento espectroeletroquímico típicos de complexos metálicos N-heterocíclicos. Esses aspectos levam a novas perspectivas relacionadas à estrutura dos compostos, pois são potencialmente interessantes para o estudo referente à formação de oxigênio singlete e para PDT. Outro direcionamento desta tese, foi o de explorar a geração de novas interfaces baseadas na formação de pares iônicos constituídos pelas espécies H2TPyPzTRu/CuTSPc em comparação com o filme da espécie catiônica H2TPyPzTRu. Através de medidas de espectroscopia de impedância eletroquímica, foram constatados mecanismos distintos de condução nos filmes formados, que pode ser ou um mecanismo misto envolvendo os complexos periféricos e o anel central da porfirazina, ou um mecanismo de condução eletrônica envolvendo somente o sistema de empilhamento π do anel central da porfirazina.
In this work, we describe the synthesis, characterization and properties of derived tetra(3,4-pyridil)porphyrazine complex containing four [Ru(bipy)2Cl]1+ groups. The electronic conjugation between the pyridinium moiety and the porphyrazine ring promote an efficient communication between the peripherical groups and central ring, which is reflected in the emission spectrum and related excitation profile. The observed behavior reveals an efficient antenna effect in the H2TPyPzTRu system. ln spite of the strong electronic coupling between the central and peripherical groups, the electronic properties of ruthenium complex were preserved, exhibiting redox potencials very close to those of free complexes. These aspects provided new perspectives of exploiting the compound strutures, particularly the oxygen singlet formation and PDT application. Another aspect focused in this investigation was the generation of new interfaces based on ion-pair formation of H2TPyPzTRu/CuTSPc, in comparison with its cationic species H2TPyPzTRu alone. By means of electrochemical impedance spectrocopy, it was shown that the conduction mecanisms in these films involve either the peripherical complex and the central porphyrazine ring.

APA, Harvard, Vancouver, ISO, and other styles

More sources

Books on the topic "Supramolecular organometallic chemistry"

1

Haiduc, Ionel. Supramolecular organometallic chemistry. Weinheim: Wiley-VCH, 1999.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

2

T, Edelmann F., ed. Supramolecular organometallic chemistry. Weinheim: Wiley-VCH, 1999.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

3

Metal-organic frameworks: Applications from catalysis to gas storage. Weinheim: Wiley-VCH, 2011.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

4

MacGillivray, Leonard. Metal-organic frameworks: Design and application. Hoboken, N.J: Wiley, 2010.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

5

The importance of Pi-interactions in crystal engineering: Frontiers in crystal engineering. Hoboken, NJ: Wiley, 2012.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

6

Edelmann, Frank Thomas, and Ionel Haiduc. Supramolecular Organometallic Chemistry. Wiley & Sons, Incorporated, John, 2008.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

7

L, Atwood J., and Lehn J. -M, eds. Comprehensive supramolecular chemistry. New York: Pergamon, 1996.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

8

Comprehensive Supramolecular Chemistry : 11-Volume Set. Pergamon, 1996.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

9

Contributors, Multiple. Comprehensive Supramolecular Chemistry : 11-Volume Set. Pergamon, 1996.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

10

Farrusseng, David. Metal-Organic Frameworks: Applications from Catalysis to Gas Storage. Wiley & Sons, Incorporated, John, 2011.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Book chapters on the topic "Supramolecular organometallic chemistry"

1

Suzaki, Yuji, Tomoko Abe, Eriko Chihara, Shintaro Murata, Masaki Horie, and Kohtaro Osakada. "Structure and Dynamic Behavior of Organometallic Rotaxanes." In Supramolecular Polymer Chemistry, 305–29. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639786.ch14.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Buriez, Olivier, Eric Labbé, and Christian Amatore. "Electrochemistry and Supramolecular Interactions of “Ferrocifen” Anticancer Drugs with Cyclodextrins and Lipid Bilayers: An Electrochemical Overview." In Advances in Organometallic Chemistry and Catalysis, 631–51. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118742952.ch47.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Haiduc, Ionel. "Supramolecular Organometallic Compounds." In Encyclopedia of Supramolecular Chemistry, 1–8. CRC Press, 2004. http://dx.doi.org/10.1081/e-esmc-120041765.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Beer, Paul D., and Elizabeth J. Hayes. "Organometallic Anion Receptors." In Encyclopedia of Supramolecular Chemistry, 1006–13. CRC Press, 2004. http://dx.doi.org/10.1081/e-esmc-120012719.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Stíbal, D., and B. Therrien. "Organometallic Chemistry in Directed Assembly." In Comprehensive Supramolecular Chemistry II, 305–29. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-409547-2.12592-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Abd‐El‐Aziz, Alaa S. "Organometallic Oligomers and Polymers." In Encyclopedia of Supramolecular Chemistry, 1014–22. CRC Press, 2004. http://dx.doi.org/10.1081/e-esmc-120019202.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

"Recent Developments in Organometallic Supramolecular Complexes as Anticancer Drugs." In Advances in Anticancer Agents in Medicinal Chemistry, edited by Cheng-He Zhou, Hui-Zhen Zhang, Sheng-Feng Cui, Jing-Song Lv, Cong-Yan Yan, Kun Wan, Yi-Yi Zhang, et al., 46–129. BENTHAM SCIENCE PUBLISHERS, 2013. http://dx.doi.org/10.2174/9781608054961113020005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Zukerman-Schpector, Julio, Ionel Haiduc, and Edward R. T. Tiekink. "Supramolecular Self-assembly of Transition Metal Carbonyl Molecules Through M–CO(Lone Pair)…π(Arene) Interactions." In Advances in Organometallic Chemistry Volume 60, 49–92. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-12-396970-5.00002-5.

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!