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[null,"1.","Record Nr.",null,"UNINA9910144282603321"]
[null,null,"Autore",null,"Haiduc Ionel"]
[null,null,"Titolo",null,"Supramolecular organometallic chemistry / / Ionel Haiduc, Frank T. Edelmann"]
[null,null,"Pubbl/distr/stampa",null,"Weinheim, [Germany] : , : Wiley-VCH, , 1999"]
[{"$nulls":4},"©1999"]
[null,null,"ISBN",null,"1-282-01042-5"]
[{"$nulls":4},"9786612010422"]
[{"$nulls":4},"3-527-61354-4"]
[{"$nulls":4},"3-527-61355-2"]
[null,null,"Descrizione fisica",null,"1 online resource (487 p.)"]
[null,null,"Disciplina",null,"547.05"]
[{"$nulls":4},"547.050442"]
[null,null,"Soggetti",null,"Supramolecular organometallic chemistry"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references at the end of each chapters and index."]
[null,null,"Nota di contenuto",null,"Supramolecular Organornetallic Chemistry; Table of Contents; 1 Basic Concepts and Principles; 1.1 Definitions; 1.1.1 Supramolecular chemistry; 1.1.2 Molecular recognition and host-guest interactions; 1.1.3 Self-assembly and self-organization; 1.2 Intermolecular Bond Types in Organometallic Supramolecular Systems; 1.2.1 Dative bonding (electron-pair donor-acceptor bonding or Lewis acid-base interactions); 1.2.2 The secondary bond concept; 1.2.3 Hydrogen-bond interactions; 1.2.4 Ionic interactions; 1.2.5 π-Bonding interactions; 2 Molecular Recognition and Host-Guest Interactions"]
[{"$nulls":4},"2.1 Organometallic Receptors and their Host-Guest Complexes2.1.1 Organomercury macrocyclic receptors; 2.1.2 Organocopper and organosilver potential receptors; 2.1.3 Organocyclosiloxane receptors; 2.1.4 Organotin macrocyclic receptors; 2.1.5 Ferrocene-containing coronands and cryptands; 2.1.5.1 Ferrocene polyoxa coronands; 2.1.5.2 Ferrocene polyaza-dxa coronands and cryptands; 2.1.5.3 Ferrocene polyaza coronands and cryptands; 2.1.5.4 Ferrocene polyoxa-thia coronands; 2.1.5.5 Ferrocene polythia coronands; 2.1.5.6 Non-cyclic ferrocene receptors; 2.1.6 Cobaltocenium receptors"]
[{"$nulls":4},"2.1.7 Other metallocene receptors2.1.8 Calixarene receptors modified with organometallic groups; 2.1.9 Organometallic cyclotriveratrylene "]
[{"$nulls":4},"receptors; 2.2 Organometallic Guests; 2.2.1 Organometallic guests in inorganic hosts; 2.2.1.1 Organometallics in zeolites and mesoporous silica; 2.2.1.2 Organometallic compounds in layered chalcogenides, oxohalides, and oxides; 2.2.2 Organometallic guests in organic hosts; 2.2.2.1 Organometallic complexes of crown ethers, cryptands and related receptors; 2.2.2.2 Organometallic molecules in cyclodextrin receptors"]
[{"$nulls":4},"2.2.2.3 Organometallics in the thiourea lattice host3 Supramolecular Self-Assembly by Dative Bonding ( Electron-Pair Donor-Acceptor or Lewis Acid-Base Interactions); 3.1 Group 12 Metals - Zinc, Cadmium, Mercury; 3.1.1 Self-assembly of organozinc compounds; 3.1.1.1 Organozinc halides; 3.1.1.2 Organozinc-oxygen compounds; 3.1.1.3 Organozinc-sulfur compounds; 3.1.1.4 Organozinc-selenium compounds; 3.1.1.5 Organozinc-nitrogen compounds; 3.1.2 Self-assembly of organocadmium compounds; 3.1.3 Self-assembly of organomercury compounds; 3.2 Group 13 Metals - Aluminum, Gallium, Indium, Thallium"]
[{"$nulls":4},"3.2.1 Self-assembly of organoaluminum compounds3.2.1.1 Organoaluminum halides; 3.2.1.2 Organoaluminum-oxygen derivatives; 3.2.1.3 Organoaluminum-sulfur derivatives; 3.2.1.4 Organoaluminum-selenium and tellurium derivatives; 3.2.1.5 Organoaluminum-nitrogen compounds; 3.2.1.6 Organoaluminum-phosphorus and organoaluminum-arsenic compounds; 3.2.2 Self-assembly of organogallium compounds; 3.2.2.1 Organogallium halides; 3.2.2.2 Organogallium-oxygen compounds; 3.2.2.3 Organogallium-sulfur compounds; 3.2.2.4 Organogallium-selenium and -tellurium compounds; 3.2.2.5 Organogallium-nitrogen compounds"]
[{"$nulls":4},"3.2.2.6 Organogallium-phosphorus, -arsenic and -antimony compounds"]
[null,null,null,"Sommario/riassunto","Supramolecular chemistry has become not only a major field of chemistry, but is also a vivid interface between chemistry, biology, physics, and materials science. Although still a relatively young field, termini such as molecular recognition, host-guest chemistry, or self-assembly are now common knowledge even for chemistry students, and research has already been honored with a Nobel Prize.This first book on supramolecular organometallic chemistry combines two areas in chemistry that are experiencing the fastest developments. It provides a comprehensive review of various organometa"]