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Journal articles on the topic 'Supramolecular organometallic chemistry'

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1

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

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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.

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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.
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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.

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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.

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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.

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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.

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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.

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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.
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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.

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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.

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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.

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11

Leclercq, Loïc, and Andreea R. Schmitzer. "Assembly of Tunable Supramolecular Organometallic Catalysts with Cyclodextrins." Organometallics 29, no. 15 (August 9, 2010): 3442–49. http://dx.doi.org/10.1021/om1006215.

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12

Sahoo, Pathik, Vedavati G. Puranik, A. K. Patra, P. U. Sastry, and Parthasarathi Dastidar. "Ferrocene based organometallic gelators: a supramolecular synthon approach." Soft Matter 7, no. 7 (2011): 3634. http://dx.doi.org/10.1039/c0sm01148g.

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13

Fan, Wenjia, Lijun Chen, and Haibo Yang. "Supramolecular Organometallic Gels Based on Neutral Platinum-Acetylide Moiety." Chinese Journal of Organic Chemistry 35, no. 3 (2015): 578. http://dx.doi.org/10.6023/cjoc201410046.

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14

Machut, Cécile, Julien Patrigeon, Sébastien Tilloy, Hervé Bricout, Frédéric Hapiot, and Eric Monflier. "Self-Assembled Supramolecular Bidentate Ligands for Aqueous Organometallic Catalysis." Angewandte Chemie International Edition 46, no. 17 (April 20, 2007): 3040–42. http://dx.doi.org/10.1002/anie.200605166.

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15

Braga, Dario, and Fabrizia Grepioni. "Intermolecular interactions and supramolecular organization in organometallic solids." Chemical Communications, no. 5 (1996): 571. http://dx.doi.org/10.1039/cc9960000571.

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16

Ding, Xue-Hua, Yong-Zheng Chang, Chang-Jin Ou, Jin-Yi Lin, Ling-Hai Xie, and Wei Huang. "Halogen bonding in the co-crystallization of potentially ditopic diiodotetrafluorobenzene: a powerful tool for constructing multicomponent supramolecular assemblies." National Science Review 7, no. 12 (August 7, 2020): 1906–32. http://dx.doi.org/10.1093/nsr/nwaa170.

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Abstract Halogen bonding is emerging as a significant driving force for supramolecular self-assembly and has aroused great interest during the last two decades. Among the various halogen-bonding donors, we take notice of the ability of 1,4-diiodotetrafluorobenzene (1,4-DITFB) to co-crystallize with diverse halogen-bonding acceptors in the range from neutral Lewis bases (nitrogen-containing compounds, N-oxides, chalcogenides, aromatic hydrocarbons and organometallic complexes) to anions (halide ions, thio/selenocyanate ions and tetrahedral oxyanions), leading to a great variety of supramolecular architectures such as discrete assemblies, 1D infinite chains and 2D/3D networks. Some of them act as promising functional materials (e.g. fluorescence, phosphorescence, optical waveguide, laser, non-linear optics, dielectric and magnetism) and soft materials (e.g. liquid crystal and supramolecular gel). Here we focus on the supramolecular structures of multicomponent complexes and their related physicochemical properties, highlight representative examples and show clearly the main directions that remain to be developed and improved in this area. From the point of view of crystal engineering and supramolecular chemistry, the complexes summarized here should give helpful information for further design and investigation of the elusive category of halogen-bonding supramolecular functional materials.
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17

McDonald, Aidan R., Davide Mores, Celso de Mello Donegá, Cornelis A. van Walree, Robertus J. M. Klein Gebbink, Martin Lutz, Anthony L. Spek, Andries Meijerink, Gerard P. M. van Klink, and Gerard van Koten. "Supramolecular Dendriphores: Anionic Organometallic Phosphors Embedded in Polycationic Dendritic Species." Organometallics 28, no. 4 (February 23, 2009): 1082–92. http://dx.doi.org/10.1021/om800226q.

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18

Desiraju, Gautam R. "The supramolecular concept as a bridge between organic, inorganic and organometallic crystal chemistry." Journal of Molecular Structure: THEOCHEM 374, no. 1-3 (January 1996): 191–98. http://dx.doi.org/10.1016/s0166-1280(96)80075-3.

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19

Haiduc, Ionel. "Thiophosphorus and related ligands in coordination, organometallic and supramolecular chemistry. A personal account." Journal of Organometallic Chemistry 623, no. 1-2 (March 2001): 29–42. http://dx.doi.org/10.1016/s0022-328x(00)00677-x.

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20

Desiraju, Gautam R. "The supramolecular concept as a bridge between organic, inorganic and organometallic crystal chemistry." Journal of Molecular Structure 374, no. 1-3 (January 1996): 191–98. http://dx.doi.org/10.1016/0022-2860(95)08932-2.

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21

Oh, Moonhyun, Gene B. Carpenter, and Dwight A. Sweigart. "Supramolecular Metal−Organometallic Coordination Networks Based on Quinonoid π-Complexes." Accounts of Chemical Research 37, no. 1 (January 2004): 1–11. http://dx.doi.org/10.1021/ar030175o.

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22

Bohle, Fabian, and Stefan Grimme. "Efficient structural and energetic screening of fullerene encapsulation in a large supramolecular double decker macrocycle." Journal of the Serbian Chemical Society 84, no. 8 (2019): 837–44. http://dx.doi.org/10.2298/jsc190701079b.

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Recently, Tanaka et al. have synthesized an organometallic supramolecular double decker macrocycle for encapsulating fullerene C70. We investigate this captivating system consisting of about 500 atoms with the robust quantum mechanical tight binding method GFN2-xTB and evaluate our computational results against an experimentally measured change in association free energy (?Ga). Further, GFN2-xTB was used to screen higher fullerene isomers and predict the best binding guest for this specific macrocycle.
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23

Mochida, Tomoyuki, Fumiko Shimizu, Hirotaka Shimizu, Kazuya Okazawa, Fuminori Sato, and Daisuke Kuwahara. "Ferrocenylpyrazole—A versatile building block for hydrogen-bonded organometallic supramolecular assemblies." Journal of Organometallic Chemistry 692, no. 9 (April 2007): 1834–44. http://dx.doi.org/10.1016/j.jorganchem.2006.11.011.

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24

Blach, Philippe, David Landy, Sophie Fourmentin, Gheorghe Surpateanu, Hervé Bricout, Anne Ponchel, Frédéric Hapiot, and Eric Monflier. "Sulfobutyl Ether-β-Cyclodextrins: Promising Supramolecular Carriers for Aqueous Organometallic Catalysis." Advanced Synthesis & Catalysis 347, no. 9 (July 2005): 1301–7. http://dx.doi.org/10.1002/adsc.200505051.

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25

Dann, Sandra E., Sean E. Durran, Mark R. J. Elsegood, Martin B. Smith, Paul M. Staniland, Salem Talib, and Sophie H. Dale. "Supramolecular chemistry of half-sandwich organometallic building blocks based on RuCl2(p-cymene)Ph2PCH2Y." Journal of Organometallic Chemistry 691, no. 23 (November 2006): 4829–42. http://dx.doi.org/10.1016/j.jorganchem.2006.07.036.

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26

Friščić, Tomislav, and Jean-Louis Do. "Chemistry 2.0: Developing a New, Solvent-Free System of Chemical Synthesis Based on Mechanochemistry." Synlett 28, no. 16 (August 17, 2017): 2066–92. http://dx.doi.org/10.1055/s-0036-1590854.

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Mechanochemistry by grinding or milling has grown from a laboratory curiosity to a versatile approach for the synthesis and discovery of molecules, materials and reactivity. Focusing on organic synthesis and the chemistry of organic solids in general, we now provide a snapshot of this exciting, rapidly developing area, with the intention to illustrate its potential in establishing a more efficient and environmentally friendly system of chemical and materials synthesis, based on solid-state transformations rather than conventional, solution-dependent chemistry.1 What is Chemistry 2.0?2 Introduction2.1 Why Mechanochemistry Now?2.2 What’s in a Mechanochemistry Laboratory?3 Liquid-Assisted Grinding (LAG): Controlling Mechanochemistry4 The Solvent-Free Research Laboratory5 Medicinal Mechanochemistry6 Exploring Molecular Recognition7 Some Myths to Dispel8 Catalytic Reactions by Mechanochemistry8.1 Catalysis and Reactivity Involving Bulk Metals8.2 Enzyme Catalysis in Mechanochemistry8.3 Coupling of Mechanochemistry, Photochemistry and Supramolecular Catalysis9 Organometallic Mechanochemistry10 New Opportunities10.1 Stoichiometric Control10.2 ‘Impossible’ Molecules10.3 Reaction Discovery by Mechanochemistry11 Energetics of Mechanochemistry12 Mechanistic Understanding13 Real-Time Reaction Monitoring14 Conclusions
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27

M, Abila Jeba Queen, Bright K.C, Mary Delphine S, and Aji Udhaya P. "Spectroscopic investigation of supramolecular organometallic compound L-threonine cadmium acetate monohydrate." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 228 (March 2020): 117802. http://dx.doi.org/10.1016/j.saa.2019.117802.

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28

Ai, Yongjian, Mengqi He, Feng Zhang, Yang Long, Yunzheng Li, Qiang Han, Mingyu Ding, Hong-bin Sun, and Qionglin Liang. "Metallo-supramolecular polymer engineered porous carbon framework encapsulated stable ultra-small nanoparticles: a general approach to construct highly dispersed catalysts." Journal of Materials Chemistry A 6, no. 34 (2018): 16680–89. http://dx.doi.org/10.1039/c8ta05369c.

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29

Moussa, Jamal, and Hani Amouri. "Supramolecular Assemblies Based on Organometallic Quinonoid Linkers: A New Class of Coordination Networks." Angewandte Chemie International Edition 47, no. 8 (February 8, 2008): 1372–80. http://dx.doi.org/10.1002/anie.200701980.

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30

Vicent, Cristian, Victor Martinez‐Agramunt, Viraj Gandhi, Carlos Larriba‐Andaluz, Dmitry G. Gusev, and Eduardo Peris. "Ion Mobility Mass Spectrometry Uncovers Guest‐Induced Distortions in a Supramolecular Organometallic Metallosquare." Angewandte Chemie International Edition 60, no. 28 (June 10, 2021): 15412–17. http://dx.doi.org/10.1002/anie.202100914.

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31

Levin, Mark D., David M. Kaphan, Cynthia M. Hong, Robert G. Bergman, Kenneth N. Raymond, and F. Dean Toste. "Scope and Mechanism of Cooperativity at the Intersection of Organometallic and Supramolecular Catalysis." Journal of the American Chemical Society 138, no. 30 (July 26, 2016): 9682–93. http://dx.doi.org/10.1021/jacs.6b05442.

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32

Plakatouras, John C. "Preface." Pure and Applied Chemistry 85, no. 2 (January 1, 2013): iv. http://dx.doi.org/10.1351/pac20138502iv.

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It is a privilege to act as the conference editor for this issue of Pure and Applied Chemistry (PAC) dedicated to the 12th Eurasia Conference on Chemical Sciences (EuAsC2S-12). The Eurasia Conferences on Chemical Sciences started in Bangkok in 1988 under the leadership of the founders, Bernd M. Rode (Austria), Hitoshi Ohtaki (Japan), and Ivano Bertini (Italy), together with Salag Dhabandana (Bangkok).During the preparation of the present issue of PAC, on 7 July 2012, Ivano Bertini, leading scientist in chemistry and biology, passed away. We will always remember him for his unselfish leadership and enormous contribution in paramagnetic NMR.The aim of the conferences is to foster friendship and exchange of knowledge between chemists in the Eurasian supercontinent as well as those in the Americas and Australia. While all previous conferences have been held in Asia or the Middle East, EuAsC2S-12 took place at the Hotel Corfu Chandris, on the island of Corfu, Greece, on 16-21 April 2012 with the aim of encouraging and enhancing the participation of European scientists and thus help to make them better known. EuAsC2S-12 was organized by the University of Ioannina on the Greek mainland with Emeritus Prof. Nick Hadjiliadis as Chair of the local organizing committee.The total number of participants was 450, with ca. 400 active delegates from 60 countries. The scientific program comprised 14 sessions, each of which was represented by invited speakers and further oral presentations on the following topics:- bioinorganic chemistry- pharmaceutical chemistry and drug design- organic synthesis and natural products- environmental and green chemistry- physical chemistry and spectroscopy- theoretical and computational chemistry- organometallic chemistry and catalysis- clinical biochemistry and molecular diagnostics- coordination chemistry and inorganic polymers- analytical and solution chemistry- supramolecular chemistry and nanomaterials- food chemistry- chemical education- polymer scienceThe scientific program, which was accompanied by a rich social activities program, included 9 plenary lectures, 214 oral presentations, and 190 poster presentations.The collection of 13 papers in this issue of PAC is a representation of the topics related to inorganic chemistry, covered in the lectures held during EuAsC2S-12. The papers represent a good cross-section of major themes ranging from traditional coordination chemistry, bio inorganic chemistry, supramolecular coordination chemistry, catalysis, and inorganic materials.The 13th Eurasia conference will be held in India in December 2014 with Prof. N. Jayaraman, Bangalore as head of the organizing committee.John C. PlakatourasConference Editor
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33

Smith, Jacob B., Andrew M. Camp, Alexandra H. Farquhar, Stewart H. Kerr, Chun-Hsing Chen, and Alexander J. M. Miller. "Organometallic Elaboration as a Strategy for Tuning the Supramolecular Characteristics of Aza-Crown Ethers." Organometallics 38, no. 22 (November 2019): 4392–98. http://dx.doi.org/10.1021/acs.organomet.9b00462.

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34

Blaszkiewicz, Claire, Hervé Bricout, Estelle Léonard, Christophe Len, David Landy, Christine Cézard, Florence Djedaïni-Pilard, Eric Monflier, and Sébastien Tilloy. "A cyclodextrin dimer as a supramolecular reaction platform for aqueous organometallic catalysis." Chemical Communications 49, no. 62 (2013): 6989. http://dx.doi.org/10.1039/c3cc43647k.

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35

Fish, Richard H., and Gérard Jaouen. "Bioorganometallic Chemistry: Structural Diversity of Organometallic Complexes with Bioligands and Molecular Recognition Studies of Several Supramolecular Hosts with Biomolecules, Alkali-Metal Ions, and Organometallic Pharmaceuticals." Organometallics 22, no. 11 (May 2003): 2166–77. http://dx.doi.org/10.1021/om0300777.

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36

Martins, Joana N., João Carlos Lima, and Nuno Basílio. "Selective Recognition of Amino Acids and Peptides by Small Supramolecular Receptors." Molecules 26, no. 1 (December 28, 2020): 106. http://dx.doi.org/10.3390/molecules26010106.

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To this day, the recognition and high affinity binding of biomolecules in water by synthetic receptors remains challenging, while the necessity for systems for their sensing, transport and modulation persists. This problematic is prevalent for the recognition of peptides, which not only have key roles in many biochemical pathways, as well as having pharmacological and biotechnological applications, but also frequently serve as models for the study of proteins. Taking inspiration in nature and on the interactions that occur between several receptors and peptide sequences, many researchers have developed and applied a variety of different synthetic receptors, as is the case of macrocyclic compounds, molecular imprinted polymers, organometallic cages, among others, to bind amino acids, small peptides and proteins. In this critical review, we present and discuss selected examples of synthetic receptors for amino acids and peptides, with a greater focus on supramolecular receptors, which show great promise for the selective recognition of these biomolecules in physiological conditions. We decided to focus preferentially on small synthetic receptors (leaving out of this review high molecular weight polymeric systems) for which more detailed and accurate molecular level information regarding the main structural and thermodynamic features of the receptor biomolecule assemblies is available.
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37

Elbjeirami, Oussama, Scott Yockel, Charles F. Campana, Angela K. Wilson, and Mohammad A. Omary. "Photophysics and Bonding in Neutral Gold(I) Organometallic Complexes with an Extended Aurophilic Supramolecular Structure." Organometallics 26, no. 10 (May 2007): 2550–60. http://dx.doi.org/10.1021/om060524t.

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38

Eckhardt, Rolf, Hilka Hanika-Heidl, and R. Dieter Fischer. "Spontaneously Organizing Metal Connectors as Supramolecular Structure Directors of Two- and Three-Dimensional Organometallic Assemblies." Chemistry - A European Journal 9, no. 8 (April 14, 2003): 1795–804. http://dx.doi.org/10.1002/chem.200390206.

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39

Kuritani, Masumi, Shohei Tashiro, and Mitsuhiko Shionoya. "Organic and Organometallic Nanofibers Formed by Supramolecular Assembly of Diamond-Shaped Macrocyclic Ligands and PdIIComplexes." Chemistry - An Asian Journal 8, no. 7 (March 28, 2013): 1368–71. http://dx.doi.org/10.1002/asia.201300209.

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40

Hannon, Michael J. "Metal-based anticancer drugs: From a past anchored in platinum chemistry to a post-genomic future of diverse chemistry and biology." Pure and Applied Chemistry 79, no. 12 (January 1, 2007): 2243–61. http://dx.doi.org/10.1351/pac200779122243.

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The field of metal-based anticancer drugs was initiated by cisplatin, one of the leading agents in clinical use. Cisplatin acts by binding to DNA and forming 1,2 intrastrand cross-links. Its importance is reflected by the fact that it is estimated that 50-70 % of cancer patients are treated with a platinum drug [7]. For some time, molecular designs in the metallo-drug field remained obdurately anchored in cis-diamine platinum(II) chemistry, but now the field is evolving rapidly with a variety of alternate and very diverse designs being explored. These designs give rise to new spectra of activity and potency and can circumvent cisplatin resistance. This critical review considers the existing clinical platinum drugs, and those currently in commercial development, alongside the new designs including ruthenium anticancer and antimetastatic drugs in clinical trials, polynuclear drugs, organometallic drugs, titanium and gallium drugs, and emerging supramolecular metallo-drugs that act on DNA by noncovalent interactions. The rapid evolution of the field is being informed by post-genomic knowledge and approaches, and further dramatic step-change breakthroughs can be expected as a result; harnessing this knowledge and responding to and taking advantage of this new environment requires integration of chemistry and biology research.
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41

Puddephatt, Richard J. "Advances in Organometallic Polymers, Ring-Opening Polymerization and the Self-Assembly of Supramolecular Polymers." Journal of Inorganic and Organometallic Polymers and Materials 15, no. 4 (December 2005): 371–88. http://dx.doi.org/10.1007/s10904-006-9012-4.

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42

Fish, Richard H. "A Bioorganometallic Chemistry Overview: From Cytochrome P450 Enzyme Metabolism of Organotin Compounds to Organorhodium-Hydroxytamoxifen Complexes with Potential Anti-Cancer Properties; A 37 Year Perspective at the Interface of Organometallic Chemistry and Biology." Australian Journal of Chemistry 63, no. 11 (2010): 1505. http://dx.doi.org/10.1071/ch10239.

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A 37 year perspective on bioorganometallic chemistry studies, which included metabolism of organotin compounds with cytochrome P450 enzymes, and their biomimics; reactions of organorhodium aqua complexes with nucleobases, nucleosides, and nucleotides; supramolecular organorhodium-nucleobase complexes as hosts for aromatic amino acid and aromatic carboxylic acid guests; regioselective reduction of NAD+ biomimics with an organorhodium hydride; tandem catalysis of an organorhodium hydride reduction to provide a 1,4-NADH biomimic for horse liver dehydrogenase stereoselective reduction of achiral ketones to chiral alcohols, and oxidation reactions with cytochrome P450 enzymes; and organorhodium-hydroxytamoxifen pharmaceuticals, will be presented. Each of these areas of bioorganometallic chemistry will be briefly discussed in this personal synopsis of the new, important, and exciting field of bioorganometallic chemistry, and its impact on metal-based drug research.
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43

Steed, Jonathan W. "Supramolecular Organometallic Chemistry Ionel Haiduc and Frank T. Edelmann. Wiley-VCH, Weinheim, 2000. ISBN 3-527-29533-X." Crystal Growth & Design 2, no. 1 (January 2002): 79. http://dx.doi.org/10.1021/cg010031l.

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44

Hissler, Muriel, Christophe Lescop, and Régis Réau. "Functional phosphorus-based π-conjugated systems: Structural diversity without multistep synthesis." Pure and Applied Chemistry 79, no. 2 (January 1, 2007): 201–12. http://dx.doi.org/10.1351/pac200779020201.

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The synthesis and properties of linear π-conjugated systems incorporating phosphole rings are described. Their supramolecular organization in the solid state can be controlled either by chemical modifications or coordination to transition metals of the phosphorus atom. Furthermore, chemical transformations of the phosphole ring allow organizing these P-chromophores in 3D assemblies exhibiting σ-π conjugation or in organometallic ferrocene-like derivatives. Phosphole-pyridine-containing π-conjugated chromophores act as P,N-chelates toward transition-metal ions, giving rise to mono- and di-nuclear complexes. The specific properties of these complexes make them valuable materials for organic light-emitting diodes (OLEDs) and interesting building blocks for the tailoring of π-conjugated systems.
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45

Mocanu, Teodora, Levente Kiss, Alexandru Sava, Sergiu Shova, Cristian Silvestru, and Marius Andruh. "Coordination polymers and supramolecular solid-state architectures constructed from an organometallic tecton, bis(4-pyridyl)mercury." Polyhedron 166 (July 2019): 7–16. http://dx.doi.org/10.1016/j.poly.2019.03.020.

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46

Moran, Moises, Carmen M. Casado, Isabel Cuadrado, and Jose Losada. "Ferrocenyl substituted octakis(dimethylsiloxy)octasilsesquioxanes: a new class of supramolecular organometallic compounds. Synthesis, characterization, and electrochemistry." Organometallics 12, no. 11 (November 1993): 4327–33. http://dx.doi.org/10.1021/om00035a018.

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47

Binkowski-Machut, Cécile, Michaël Canipelle, Hervé Bricout, Sébastien Tilloy, Frédéric Hapiot, and Eric Monflier. "Supramolecular Trapping of Phosphanes by Cyclodextrins: A General Approach to Generate Phosphane Coordinatively Unsaturated Organometallic Complexes." European Journal of Inorganic Chemistry 2006, no. 8 (April 2006): 1611–19. http://dx.doi.org/10.1002/ejic.200500925.

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48

Moussa, Mehdi Elsayed, Jana Schiller, Michael Seidl, Pavel A. Shelyganov, and Manfred Scheer. "Discrete and polymeric organometallic-organic assemblies based on the diarsene complex [(Cp)2Mo2(CO)4(μ,η2-As2)], AgPF6 and N-donor organic molecules." New Journal of Chemistry 45, no. 4 (2021): 1800–1804. http://dx.doi.org/10.1039/d0nj05959e.

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Abstract:
The first mixed-ligand self-assembly reactions of the diarsene complex [Cp2Mo2(CO)4(μ,η2-As2)] and N-donor organic molecules in the presence of AgPF6 allow for the synthesis of two discrete and four polymeric supramolecular aggregates.
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49

Elsayed Moussa, Mehdi, Pavel A. Shelyganov, Brian Wegley, Michael Seidl, and Manfred Scheer. "The Potential of the Diphosphorus Complex [Cp2 W2 (CO)4 (η2 -P2 )] as an Organometallic Connecter in Supramolecular Chemistry." European Journal of Inorganic Chemistry 2019, no. 39-40 (July 24, 2019): 4241–48. http://dx.doi.org/10.1002/ejic.201900580.

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50

Torque, Christophe, Benoît Sueur, Jérôme Cabou, Hervé Bricout, Frédéric Hapiot, and Eric Monflier. "Substrate-selective aqueous organometallic catalysis. How small water-soluble organic molecules enhance the supramolecular discrimination." Tetrahedron 61, no. 20 (May 2005): 4811–17. http://dx.doi.org/10.1016/j.tet.2005.03.017.

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