Chalcogen chemistry :: fundamentals and applications /
Covering organic and inorganic synthesis, structural properties, coordination chemistry and computational modelling, all key classes of chalcogen compounds are illustrated.
Gespeichert in:
| Weitere Verfasser: | , , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
London :
Royal Society of Chemistry,
[2023]
|
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Zusammenfassung: | Covering organic and inorganic synthesis, structural properties, coordination chemistry and computational modelling, all key classes of chalcogen compounds are illustrated. |
| Beschreibung: | 1 online resource (xxii, 728 pages) : illustrations |
| Bibliographie: | Includes bibliographical references and index. |
| ISBN: | 9781839167386 1839167386 9781839167393 1839167394 |
Internformat
MARC
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| 003 | OCoLC | ||
| 005 | 20241004212047.0 | ||
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| 049 | |a MAIN | ||
| 245 | 0 | 0 | |a Chalcogen chemistry : |b fundamentals and applications / |c edited by Vito Lippolis, Claudio Santi, Eder J. Lenardão and Antonio L. Braga. |
| 264 | 1 | |a London : |b Royal Society of Chemistry, |c [2023] | |
| 300 | |a 1 online resource (xxii, 728 pages) : |b illustrations | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 504 | |a Includes bibliographical references and index. | ||
| 505 | 2 | |a Chapter 1: Carbonyl Chalcogenide Cluster-based Polymers -- 1.1 Introduction -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3.1 Te-Mn Cluster-based Carbonyl Polymers -- 1.3.2 S-Re Rectangular Carbonyl Polymers -- 1.4 Group 8 Metal Carbonyl Chalcogenide Coordination Polymers -- 1.4.1 S-Fe Cluster-based Carbonyl Polymers | |
| 505 | 8 | |a 1.4.2 EFe3 (E=Te, Se, S) -- Cluster-based Carbonyl Polymers -- 1.4.3 Mixed Group 15 and 16 Fe Carbonyl Supramolecules -- 1.4.4 Ru Telluride Carbonyl Polymer -- 1.5 Potential Applications -- 1.5.1 Semiconducting Behaviors -- 1.5.2 Photodegradation -- 1.5.3 Magnetic Properties -- 1.5.4 Catalysis -- 1.5.5 Adsorption/Desorption Properties -- 1.6 Concluding Remarks -- Acknowledgments -- References -- Chapter 2: Chalcogenocarbonyl and Chalcogenonitrosyl Metal Complexes -- 2.1 Introduction -- 2.2 Chalcogenocarbonyl (CE) Complexes -- 2.3 New Thiocarbonyl (CS) | |
| 505 | 8 | |a Complexes Reported after 2008 -- 2.3 New Thiocarbonyl (CS&rpar -- Complexes Reported after 2008 -- 2.4 Selenocarbonyl (CS) Complexes -- 2.4.1 Complexes Featuring Terminal Coordinated CSe -- 2.4.1.1 Synthesis -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.3 List of Complexes Featuring Terminal Coordinated CSe and Characterized by X-ray Diffraction Studies -- 2.4.2 Complexes Featuring Bridging Coordinated CSe -- 2.4.2.1 Complexes Featuring Symmetric Bridging CSe | |
| 505 | 8 | |a 2.4.2.2 Complexes Featuring End-on/Side-on Bridging CSe -- 2.4.2.3 Complexes Featuring Bridging End-on/End-on CSe -- 2.4.2.4 Complexes Featuring Bridging ç3- and ç4-CSe -- 2.4.2.5 List of Complexes Featuring Bridging CSe -- 2.5 Tellurocarbonyl (CT) Complexes -- 2.5.1 Complexes Featuring Terminal Coordinated CTe -- 2.5.1.1 Synthesis -- 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe | |
| 505 | 8 | |a 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe -- 2.5.2 Complexes Featuring Bridging Coordinated CTe -- 2.5.3 List of all CTe Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.7 Chalcogenonitrosyl (NE) Complexes -- 2.8 Thionitrosyl (NS) Complexes -- 2.8.1 Synthesis -- 2.8.2 Reactions -- 2.8.3 List of NS Complexes Characterized by an X-ray Diffraction Study -- 2.9 Selenonitrosyl (NS) | |
| 520 | |a Covering organic and inorganic synthesis, structural properties, coordination chemistry and computational modelling, all key classes of chalcogen compounds are illustrated. | ||
| 588 | 0 | |a Online resource; title from digital title page (viewed on April 28, 2023). | |
| 650 | 0 | |a Chalcogens. |0 http://id.loc.gov/authorities/subjects/sh2002008811 | |
| 650 | 6 | |a Chalcogènes. | |
| 650 | 7 | |a Chalcogens |2 fast | |
| 700 | 1 | |a Lippolis, Vito, |e editor. | |
| 700 | 1 | |a Santi, Claudio, |e editor. | |
| 700 | 1 | |a Lenardão, Eder J., |e editor. | |
| 700 | 1 | |a Braga, Antonio L., |e editor. | |
| 776 | 0 | 8 | |i Print version: |z 1839164220 |z 9781839164224 |w (OCoLC)1334884869 |
| 856 | 4 | 0 | |l FWS01 |p ZDB-4-EBA |q FWS_PDA_EBA |u https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=3556158 |3 Volltext |
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Datensatz im Suchindex
| DE-BY-FWS_katkey | ZDB-4-EBA-on1370526983 |
|---|---|
| _version_ | 1816882568534949889 |
| adam_text | |
| any_adam_object | |
| author2 | Lippolis, Vito Santi, Claudio Lenardão, Eder J. Braga, Antonio L. |
| author2_role | edt edt edt edt |
| author2_variant | v l vl c s cs e j l ej ejl a l b al alb |
| author_facet | Lippolis, Vito Santi, Claudio Lenardão, Eder J. Braga, Antonio L. |
| building | Verbundindex |
| bvnumber | localFWS |
| callnumber-first | Q - Science |
| callnumber-label | QD169 |
| callnumber-raw | QD169.C5 C43 2023 |
| callnumber-search | QD169.C5 C43 2023 |
| callnumber-sort | QD 3169 C5 C43 42023 |
| callnumber-subject | QD - Chemistry |
| collection | ZDB-4-EBA |
| contents | Chapter 1: Carbonyl Chalcogenide Cluster-based Polymers -- 1.1 Introduction -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3.1 Te-Mn Cluster-based Carbonyl Polymers -- 1.3.2 S-Re Rectangular Carbonyl Polymers -- 1.4 Group 8 Metal Carbonyl Chalcogenide Coordination Polymers -- 1.4.1 S-Fe Cluster-based Carbonyl Polymers 1.4.2 EFe3 (E=Te, Se, S) -- Cluster-based Carbonyl Polymers -- 1.4.3 Mixed Group 15 and 16 Fe Carbonyl Supramolecules -- 1.4.4 Ru Telluride Carbonyl Polymer -- 1.5 Potential Applications -- 1.5.1 Semiconducting Behaviors -- 1.5.2 Photodegradation -- 1.5.3 Magnetic Properties -- 1.5.4 Catalysis -- 1.5.5 Adsorption/Desorption Properties -- 1.6 Concluding Remarks -- Acknowledgments -- References -- Chapter 2: Chalcogenocarbonyl and Chalcogenonitrosyl Metal Complexes -- 2.1 Introduction -- 2.2 Chalcogenocarbonyl (CE) Complexes -- 2.3 New Thiocarbonyl (CS) Complexes Reported after 2008 -- 2.3 New Thiocarbonyl (CS&rpar -- Complexes Reported after 2008 -- 2.4 Selenocarbonyl (CS) Complexes -- 2.4.1 Complexes Featuring Terminal Coordinated CSe -- 2.4.1.1 Synthesis -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.3 List of Complexes Featuring Terminal Coordinated CSe and Characterized by X-ray Diffraction Studies -- 2.4.2 Complexes Featuring Bridging Coordinated CSe -- 2.4.2.1 Complexes Featuring Symmetric Bridging CSe 2.4.2.2 Complexes Featuring End-on/Side-on Bridging CSe -- 2.4.2.3 Complexes Featuring Bridging End-on/End-on CSe -- 2.4.2.4 Complexes Featuring Bridging ç3- and ç4-CSe -- 2.4.2.5 List of Complexes Featuring Bridging CSe -- 2.5 Tellurocarbonyl (CT) Complexes -- 2.5.1 Complexes Featuring Terminal Coordinated CTe -- 2.5.1.1 Synthesis -- 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe -- 2.5.2 Complexes Featuring Bridging Coordinated CTe -- 2.5.3 List of all CTe Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.7 Chalcogenonitrosyl (NE) Complexes -- 2.8 Thionitrosyl (NS) Complexes -- 2.8.1 Synthesis -- 2.8.2 Reactions -- 2.8.3 List of NS Complexes Characterized by an X-ray Diffraction Study -- 2.9 Selenonitrosyl (NS) |
| ctrlnum | (OCoLC)1370526983 |
| dewey-full | 546/.72 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 546 - Inorganic chemistry |
| dewey-raw | 546/.72 |
| dewey-search | 546/.72 |
| dewey-sort | 3546 272 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie |
| format | Electronic eBook |
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| id | ZDB-4-EBA-on1370526983 |
| illustrated | Illustrated |
| indexdate | 2024-11-27T13:30:41Z |
| institution | BVB |
| isbn | 9781839167386 1839167386 9781839167393 1839167394 |
| language | English |
| oclc_num | 1370526983 |
| open_access_boolean | |
| owner | MAIN DE-863 DE-BY-FWS |
| owner_facet | MAIN DE-863 DE-BY-FWS |
| physical | 1 online resource (xxii, 728 pages) : illustrations |
| psigel | ZDB-4-EBA |
| publishDate | 2023 |
| publishDateSearch | 2023 |
| publishDateSort | 2023 |
| publisher | Royal Society of Chemistry, |
| record_format | marc |
| spelling | Chalcogen chemistry : fundamentals and applications / edited by Vito Lippolis, Claudio Santi, Eder J. Lenardão and Antonio L. Braga. London : Royal Society of Chemistry, [2023] 1 online resource (xxii, 728 pages) : illustrations text txt rdacontent computer c rdamedia online resource cr rdacarrier Includes bibliographical references and index. Chapter 1: Carbonyl Chalcogenide Cluster-based Polymers -- 1.1 Introduction -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3.1 Te-Mn Cluster-based Carbonyl Polymers -- 1.3.2 S-Re Rectangular Carbonyl Polymers -- 1.4 Group 8 Metal Carbonyl Chalcogenide Coordination Polymers -- 1.4.1 S-Fe Cluster-based Carbonyl Polymers 1.4.2 EFe3 (E=Te, Se, S) -- Cluster-based Carbonyl Polymers -- 1.4.3 Mixed Group 15 and 16 Fe Carbonyl Supramolecules -- 1.4.4 Ru Telluride Carbonyl Polymer -- 1.5 Potential Applications -- 1.5.1 Semiconducting Behaviors -- 1.5.2 Photodegradation -- 1.5.3 Magnetic Properties -- 1.5.4 Catalysis -- 1.5.5 Adsorption/Desorption Properties -- 1.6 Concluding Remarks -- Acknowledgments -- References -- Chapter 2: Chalcogenocarbonyl and Chalcogenonitrosyl Metal Complexes -- 2.1 Introduction -- 2.2 Chalcogenocarbonyl (CE) Complexes -- 2.3 New Thiocarbonyl (CS) Complexes Reported after 2008 -- 2.3 New Thiocarbonyl (CS&rpar -- Complexes Reported after 2008 -- 2.4 Selenocarbonyl (CS) Complexes -- 2.4.1 Complexes Featuring Terminal Coordinated CSe -- 2.4.1.1 Synthesis -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.3 List of Complexes Featuring Terminal Coordinated CSe and Characterized by X-ray Diffraction Studies -- 2.4.2 Complexes Featuring Bridging Coordinated CSe -- 2.4.2.1 Complexes Featuring Symmetric Bridging CSe 2.4.2.2 Complexes Featuring End-on/Side-on Bridging CSe -- 2.4.2.3 Complexes Featuring Bridging End-on/End-on CSe -- 2.4.2.4 Complexes Featuring Bridging ç3- and ç4-CSe -- 2.4.2.5 List of Complexes Featuring Bridging CSe -- 2.5 Tellurocarbonyl (CT) Complexes -- 2.5.1 Complexes Featuring Terminal Coordinated CTe -- 2.5.1.1 Synthesis -- 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe -- 2.5.2 Complexes Featuring Bridging Coordinated CTe -- 2.5.3 List of all CTe Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.7 Chalcogenonitrosyl (NE) Complexes -- 2.8 Thionitrosyl (NS) Complexes -- 2.8.1 Synthesis -- 2.8.2 Reactions -- 2.8.3 List of NS Complexes Characterized by an X-ray Diffraction Study -- 2.9 Selenonitrosyl (NS) Covering organic and inorganic synthesis, structural properties, coordination chemistry and computational modelling, all key classes of chalcogen compounds are illustrated. Online resource; title from digital title page (viewed on April 28, 2023). Chalcogens. http://id.loc.gov/authorities/subjects/sh2002008811 Chalcogènes. Chalcogens fast Lippolis, Vito, editor. Santi, Claudio, editor. Lenardão, Eder J., editor. Braga, Antonio L., editor. Print version: 1839164220 9781839164224 (OCoLC)1334884869 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=3556158 Volltext |
| spellingShingle | Chalcogen chemistry : fundamentals and applications / Chapter 1: Carbonyl Chalcogenide Cluster-based Polymers -- 1.1 Introduction -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.2 Group 6 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3 Group 7 Carbonyl Chalcogenide Coordination Polymers -- 1.3.1 Te-Mn Cluster-based Carbonyl Polymers -- 1.3.2 S-Re Rectangular Carbonyl Polymers -- 1.4 Group 8 Metal Carbonyl Chalcogenide Coordination Polymers -- 1.4.1 S-Fe Cluster-based Carbonyl Polymers 1.4.2 EFe3 (E=Te, Se, S) -- Cluster-based Carbonyl Polymers -- 1.4.3 Mixed Group 15 and 16 Fe Carbonyl Supramolecules -- 1.4.4 Ru Telluride Carbonyl Polymer -- 1.5 Potential Applications -- 1.5.1 Semiconducting Behaviors -- 1.5.2 Photodegradation -- 1.5.3 Magnetic Properties -- 1.5.4 Catalysis -- 1.5.5 Adsorption/Desorption Properties -- 1.6 Concluding Remarks -- Acknowledgments -- References -- Chapter 2: Chalcogenocarbonyl and Chalcogenonitrosyl Metal Complexes -- 2.1 Introduction -- 2.2 Chalcogenocarbonyl (CE) Complexes -- 2.3 New Thiocarbonyl (CS) Complexes Reported after 2008 -- 2.3 New Thiocarbonyl (CS&rpar -- Complexes Reported after 2008 -- 2.4 Selenocarbonyl (CS) Complexes -- 2.4.1 Complexes Featuring Terminal Coordinated CSe -- 2.4.1.1 Synthesis -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.2 Reactions of Complexes Featuring Terminal Coordinated CSe -- 2.4.1.3 List of Complexes Featuring Terminal Coordinated CSe and Characterized by X-ray Diffraction Studies -- 2.4.2 Complexes Featuring Bridging Coordinated CSe -- 2.4.2.1 Complexes Featuring Symmetric Bridging CSe 2.4.2.2 Complexes Featuring End-on/Side-on Bridging CSe -- 2.4.2.3 Complexes Featuring Bridging End-on/End-on CSe -- 2.4.2.4 Complexes Featuring Bridging ç3- and ç4-CSe -- 2.4.2.5 List of Complexes Featuring Bridging CSe -- 2.5 Tellurocarbonyl (CT) Complexes -- 2.5.1 Complexes Featuring Terminal Coordinated CTe -- 2.5.1.1 Synthesis -- 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe 2.5.1.2 Reactions of Complexes Featuring Terminal Coordinated CTe -- 2.5.2 Complexes Featuring Bridging Coordinated CTe -- 2.5.3 List of all CTe Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.6 Comparison of a Series of CE (E=O, S, Se, T) Complexes -- 2.7 Chalcogenonitrosyl (NE) Complexes -- 2.8 Thionitrosyl (NS) Complexes -- 2.8.1 Synthesis -- 2.8.2 Reactions -- 2.8.3 List of NS Complexes Characterized by an X-ray Diffraction Study -- 2.9 Selenonitrosyl (NS) Chalcogens. http://id.loc.gov/authorities/subjects/sh2002008811 Chalcogènes. Chalcogens fast |
| subject_GND | http://id.loc.gov/authorities/subjects/sh2002008811 |
| title | Chalcogen chemistry : fundamentals and applications / |
| title_auth | Chalcogen chemistry : fundamentals and applications / |
| title_exact_search | Chalcogen chemistry : fundamentals and applications / |
| title_full | Chalcogen chemistry : fundamentals and applications / edited by Vito Lippolis, Claudio Santi, Eder J. Lenardão and Antonio L. Braga. |
| title_fullStr | Chalcogen chemistry : fundamentals and applications / edited by Vito Lippolis, Claudio Santi, Eder J. Lenardão and Antonio L. Braga. |
| title_full_unstemmed | Chalcogen chemistry : fundamentals and applications / edited by Vito Lippolis, Claudio Santi, Eder J. Lenardão and Antonio L. Braga. |
| title_short | Chalcogen chemistry : |
| title_sort | chalcogen chemistry fundamentals and applications |
| title_sub | fundamentals and applications / |
| topic | Chalcogens. http://id.loc.gov/authorities/subjects/sh2002008811 Chalcogènes. Chalcogens fast |
| topic_facet | Chalcogens. Chalcogènes. Chalcogens |
| url | https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=3556158 |
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