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Synthesis and Modifications of Porphyrinoids de Roberto Paolesse

Synthesis and Modifications of Porphyrinoids: Topics in Heterocyclic Chemistry, cartea 33

Editat de Roberto Paolesse
en Limba Engleză Hardback – 26 noi 2013
The McMurry Reaction in Porphyrinoid Chemistry, by Kevin M. Smith

Meso-tetraarylporphyrins: synthetic strategies and reactivity profiles based on nitro/amino substituents, by Maria da Graça Neves

Functionalization of corroles, by José Cavaleiro

Degradation pathways for porphyrinoids, by  Jacek Wojaczynski
Synthetic routes to porphyrinoids, by Sara Nardis

Recent developments of non covalent porphyrin assemblies, by Donato Monti

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Specificații

ISBN-13: 9783642385322
ISBN-10: 364238532X
Pagini: 304
Ilustrații: VII, 296 p. 50 illus., 23 illus. in color.
Dimensiuni: 155 x 235 x 25 mm
Greutate: 0.6 kg
Ediția:2014
Editura: Springer Berlin, Heidelberg
Colecția Springer
Seria Topics in Heterocyclic Chemistry

Locul publicării:Berlin, Heidelberg, Germany

Public țintă

Research

Cuprins

The McMurry Reaction in Porphyrinoid Chemistry.- Meso-tetraarylporphyrins: synthetic strategies and reactivity profiles based on nitro/amino substituents.- Functionalization of corroles.- Degradation pathways for porphyrinoids.- Synthetic routes to porphyrinoids.- Recent developments of non covalent porphyrin assemblies.

Textul de pe ultima copertă

Kevin M. Smith
The McMurry Reaction in Porphyrinoid Chemistry
Maria da Graça Neves
Meso-tetraarylporphyrins: synthetic strategies and reactivity profiles based on nitro/amino substituents
José Cavaleiro
Functionalization of corroles
Jacek Wojaczynski
Degradation pathways for porphyrinoids
Sara Nardis
Synthetic routes to porphyrinoids
Donato Monti
Recent developments of non covalent porphyrin assemblies

Caracteristici

Heterocyclic chemistry is the biggest branch of chemistry covering two-third of the chemical literature The series covers hot topics of frontier research summarized by reputed scientists in the field Our review series is topic related Online version available on SpringerLink.com Includes supplementary material: sn.pub/extras