Recent advances in organometallic chemistry : synthetic, mechanistic and medicinal perspective /

Recent Advances in Organometallic Chemistry: Synthetic, Mechanistic and Medicinal Perspective highlights recent advancements in the field of organometallic chemistry.Containing essential information for researchers and advanced-level students, especially those working in chemical synthesis, the book...

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Bibliographic Details
Corporate Author: ScienceDirect (Online service)
Other Authors: Ansari, Azaj, Kumar, Vinod
Format: eBook
Language:English
Published: Amsterdam : Elsevier, 2024.
Subjects:
Online Access:Connect to the full text of this electronic book
Table of Contents:
  • 5.3.2 Iron-catalyzed C-H activation
  • 5.3.3 Rhodium-catalyzed C-H activation
  • 5.4 Future prospective and scope
  • 5.5 Summary
  • References
  • 6 Organotransition metal chemistry in asymmetric catalysis mediated by different transition metal N-heterocyclic carbene co...
  • 6.1 Introduction
  • 6.2 Fundamental principles
  • 6.3 Common methods of preparation
  • 6.4 Mechanism involved
  • 6.5 Recent developments with examples
  • 6.6 Applications in emerging fields
  • 6.7 Future prospective and scope
  • 6.8 Summary
  • 6.9 Problems with solutions
  • 6.10 Objective type questions
  • References
  • 7 Organophosphorus compounds: recent developments and future perspective
  • 7.1 Introduction
  • 7.2 Fundamental principles
  • 7.2.1 Phosphorus-based ligands
  • 7.2.2 Classification of phosphorus-based ligands
  • 7.3 Common methods of preparation
  • 7.3.1 Pincer ligands
  • 7.3.2 Synthesis of pincer complexes
  • 7.3.2.1 C-H bond activation
  • 7.3.3 Oxidative addition to aryl halide bond
  • 7.3.4 Trans-metallation
  • 7.3.5 Trans-cyclometallation
  • 7.4 Classification of pincer complexes
  • 7.4.1 Transition metal chemistry of pincer ligands
  • 7.4.1.1 PCP pincer complexes
  • 7.4.1.2 PNP pincer complexes
  • 7.4.2 Application of tridentate chelating pincer complexes in catalysis
  • 7.4.2.1 Heck cross-coupling reactions
  • 7.4.2.2 Asymmetric allylation of sulfonimines
  • 7.4.2.3 Hydrophosphination reaction
  • 7.4.3 Chiral tridentate chelating pincer complexes
  • 7.4.4 Aminophosphines
  • 7.4.4.1 Cyclodiphosphazanes
  • 7.4.4.2 Cis/trans isomerization
  • 7.4.4.3 Synthesis of cyclodiphosphazanes
  • 7.4.4.4 Reactivity of cyclodiphosphazanes
  • 7.4.4.5 Macrocyclic cyclodiphosphazane derivatives
  • 7.4.5 Phosphacyclophanes
  • 7.5 Summary
  • 7.6 Problems with solutions
  • 7.7 Objective-type questions
  • References.
  • 8 Synthesis of silicon and germanium organometallic compounds and their applications in catalysis
  • 8.1 Introduction
  • 8.2 Synthesizing of silicon and germanium organometallic compounds
  • 8.2.1 Direct synthesis
  • 8.2.2 Hydrosilylation
  • 8.2.3 Silenes
  • 8.2.4 Silicones, silyl ethers, silanols, siloxanes, and siloxides
  • 8.2.5 Bonding through carbon
  • 8.3 Catalysis
  • 8.4 Future prospective and scope
  • 8.5 Summary
  • 8.6 Problems with solutions
  • 8.7 Objective type questions
  • References
  • 9 Sensing application of organometallic compounds
  • 9.1 Introduction
  • 9.2 Fundamental principles
  • 9.3 Common methods of preparation
  • 9.4 Mechanism involved
  • 9.4.1 Ligand substitution
  • 9.4.2 Oxidative addition
  • 9.4.3 Concerted track based
  • 9.5 Recent developments with examples
  • 9.6 Applications in emerging fields
  • 9.6.1 Chemical sensor
  • 9.6.2 Gas sensor
  • 9.6.3 Optical sensor
  • 9.6.4 Biochemical sensor
  • 9.7 Future prospective and scope
  • 9.8 Summary
  • 9.9 Problems with solutions
  • 9.10 Objective type questions
  • References
  • 10 Bioorganometallic chemistry: a new horizon on organometallic landscape
  • 10.1 Introduction
  • 10.2 Shift from platinum metal based therapeutics to other bio-compatible less toxic nonplatinum complexes
  • 10.2.1 Anticancerous properties of iron complexes
  • 10.2.2 Anticancer properties of copper complexes
  • 10.2.3 Anticancer properties of ruthenium complexes
  • 10.2.3.1 Substitution modulated anticancer activity of Half-sandwich ruthenium (II) complexes with heterocyclic ancillary l...
  • 10.2.4 Anticancer properties of gold complexes
  • 10.2.5 Anticancer properties of rhodium and iridium complexes
  • 10.3 Organoselenium compounds as potent chemotherapeutic agents
  • 10.3.1 Inorganic selenium compounds
  • 10.3.2 Organic selenium compounds
  • 10.3.3 Selenocysteine
  • 10.3.4 Selol.
  • 10.3.5 Seleninic acids
  • 10.3.6 Selenophene-based derivatives
  • 10.3.7 1,2-Benzisoselenazole-3[2H]-one derivatives
  • 10.3.8 Analysis of anticancer property of selenium-bearing 4-anilinoquinazoline compounds
  • 10.3.8.1 Anticancer agent
  • 10.3.9 Evaluation of indole chalcone and diarylketone derivatives containing selenium as tubulin polymerization inhibitory ...
  • 10.3.9.1 Effect of diarylketone selenium derivative(compound-36) on the advancement of cell apoptosis
  • 10.3.10 Chemopreventive applications of isoselenocyanate compounds
  • 10.4 Other biological activities of organoselenium compounds
  • 10.4.1 GPx activity
  • 10.4.1.1 Catalytic GPx-like activity of 2,7-dialkoxy-substituted naphthalene-1,8-peri diselenides
  • 10.4.1.2 pH-sensitive organoselenium compounds as pH-responsive glutathione peroxidase mimics
  • 10.4.1.2.1 Mechanistic study
  • 10.4.1.3 Enhanced activity as glutathione peroxidase mimics when benzo[d]isoselenazol-3-ones are combined with sterically h...
  • 10.4.2 Anti-Alzheimer activity
  • 10.4.2.1 Selenyl-dihydrofurans as anti-Alzheimer agents
  • 10.4.2.2 Selenodihydropyrimidinones as potential multi-targeted treatments for Alzheimer's disease
  • 10.4.2.3 AChE inhibitory activity
  • 10.4.3 Cytoprotection
  • 10.4.3.1 Organoselenium antioxidant compounds with cytoprotective effects
  • 10.4.3.2 Bromo substituted diselenide compounds potential to scavenge ROS
  • 10.4.4 Insecticidal activity
  • 10.4.4.1 Selenoethers and their insecticidal activities
  • 10.4.4.2 2,2-Difluoro-1,3-benzoxathioles (selenoles)with insecticidal activities
  • 10.4.4.3 Selenium-containing imidazolium ionic liquids with antibacterial activity
  • 10.4.4.4 Cyclization of Z-selenoenynes by iron(III)-PhSeSePh results in selenophenes with antidepressant-like activity
  • 10.5 Different plausible mechanisms of action for bioorganometallic complexes.