The Synthesis and Properties of Conjugated Porphyrin Oligomers and Polymers

The Synthesis and Properties of Conjugated Porphyrin Oligomers and Polymers PDF Author: Thomas E. O. Screen
Publisher:
ISBN:
Category : Porphyrins
Languages : en
Pages : 456

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The Synthesis and Properties of Conjugated Porphyrin Oligomers and Polymers

The Synthesis and Properties of Conjugated Porphyrin Oligomers and Polymers PDF Author: Thomas E. O. Screen
Publisher:
ISBN:
Category : Porphyrins
Languages : en
Pages : 456

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Electronic Communication in Heterometallated Porphyrin Oligomers

Electronic Communication in Heterometallated Porphyrin Oligomers PDF Author: Jonathan Cremers
Publisher: Springer Nature
ISBN: 3030391019
Category : Science
Languages : en
Pages : 294

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This book cuts across the divisions of organic, inorganic, and physical chemistry. It describes new methods for creating π-conjugated porphyrin oligomers with precisely defined sequences of zinc and copper metal cations, and how EPR spectroscopy was used to investigate the dipolar and exchange coupling between the paramagnetic copper(II) centres. Porphyrins are a group of heterocyclic macrocycle organic compounds that play an important role in our everyday life and can for example be found in blood where they form a red complex with iron (haem). Various metallic elements can be inserted into a porphyrin and changing the coordinated metal is an excellent way to influence the chemical and physical properties of these molecules. Focusing on 3 metals - zinc, magnesium and copper - the author established new methods for creating π-conjugated porphyrin oligomers and lastly presents the synthesis and investigation of two novel porphyrin nanoballs. Giving the template-directed strategy the author developed for constructing these molecules, this work could provide access to other related nano-cages.

Conjugated Porphyrin Oligomers

Conjugated Porphyrin Oligomers PDF Author: Joakim Kärnbratt
Publisher:
ISBN: 9789173854993
Category :
Languages : en
Pages : 60

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Synthesis of Novel Conjugated Porphyrins and Porphyrin Oligomers

Synthesis of Novel Conjugated Porphyrins and Porphyrin Oligomers PDF Author: Aurélie Stallivieri
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Probing the Effects of Conformation on the Photophysics of Conjugated Porphyrin Oligomers

Probing the Effects of Conformation on the Photophysics of Conjugated Porphyrin Oligomers PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 45

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Influence of Conformations and Geometries on the Photophysical Properties of Conjugated Porphyrin Oligomers

Influence of Conformations and Geometries on the Photophysical Properties of Conjugated Porphyrin Oligomers PDF Author: Joakim Kärnbratt
Publisher:
ISBN:
Category :
Languages : en
Pages : 24

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Conjugated Polymer Synthesis

Conjugated Polymer Synthesis PDF Author: Yoshiki Chujo
Publisher: John Wiley & Sons
ISBN: 3527632689
Category : Technology & Engineering
Languages : en
Pages : 333

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Edited and authored by top international experts, this first book on conjugated polymers with a focus on synthesis provides a detailed overview of all modern synthetic methods for these highly interesting compounds. As such, it describes every important compound class, including polysilanes, organoboron compounds, and ferrocene-containing conjugated polymers. An indispensable source for every synthetic polymer chemist.

Synthesis of New Conjugated Meso Porphyrin Dendrimers and Oligomers and Study of Their Optical Properties

Synthesis of New Conjugated Meso Porphyrin Dendrimers and Oligomers and Study of Their Optical Properties PDF Author: Dandan Yao
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

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During this thesis, we have worked on the synthesis and characterization of new compounds using the porphyrin macrocycle as a starting material. The aim, after synthesis, was to study the photophysical properties of these new molecules. More precisely, we have synthesized and characterized three groups of fluorenyl-porphyrin dendrimers and two oligomers in conjugated structures. Their correlation on optical property-structure have been discussed in detail, as well as the energy transfer processes from the conjugated dendron donor to porphyrin acceptor. In the first chapter, we introduce the general background of the porphyrin chemistry based on three aspects: (i) structure, (ii) optical properties and (iii) synthetic methods. We further review prior porphyrin studies done in our group and propose new molecular designs based on these results. In the second chapter, we study the influence of substitution position and nature of the antennae on the central core. Two groups of new TPP-cored porphyrin dendrimers were synthesized according to different substituted positions on the peripheral phenyl rings: para-substituted series TPP1, TPP2 and TPP3, and meta-substituted ones TPP4, TPP5 and TPP6. All have conjugated dendrons with bridged phenyl-alkynyl and are terminated by fluorenyl groups. In the third chapter, we study the influence of positions of light absorbers. To this aim, a series of TFP-cored porphyrin dendrimers presenting fluorenyls in conjugated dendrons on different positions is reported (core fluorenyl, bridging fluorenyl and terminal fluorenyl): TFP1, TFP2 and TFP3. The core fluorenyl mainly influences emission peaks and quantum yield, while the bridging fluorenyl and terminal fluorenyl have a large effect on the dendron absorption and on the energy transfer efficiency. Thus, for the largest dendrimer TFP3, dendron emission is not totally quenched by long distance energy transfer process when exciting the peripheral dendrons. In the fourth chapter, we study the influence of linkages in the Dendron. Thus, two new porphyrin dendrimers with bridged vinyl, TPP-D and TFP-D, were synthesized and compared to analogues with alkynyl bridged TPP-T and TFP-T. Vinyl and alkynyl bridges are shown to influence the optical properties of the porphyrin dendrimers to a certain extent depending on the substituted positions. Finally, in the last chapter, two oligomers with n-butyl substituted TFP as terminal group, a linear dimer and a star - shaped trimer, were synthesized from the same porphyrin monomer.

Synthesis and Near-Infrared Luminescence of a Deuterated Conjugated Porphyrin Dimer for Probing the Mechanism of Non-Radiative Deactivation (Postprint).

Synthesis and Near-Infrared Luminescence of a Deuterated Conjugated Porphyrin Dimer for Probing the Mechanism of Non-Radiative Deactivation (Postprint). PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 9

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Beta-meso-beta-Fused porphyrin oligomers have many attractive photophysical features such as strong absorption in the near-IR at wavelengths greater than 1000 nm, and high two-photon cross sections. However their ultrafast S(sub-1)-S(sub-0) deactivation limits potential applications. We have synthesised a deuterated fused porphyrin dimer to test whether deuteration influences the rate of non-radiative deactivation. An efficient synthetic strategy was developed, starting with deuteration of dipyrromethane. Deuteration of the zinc porphyrin dimer does not affect its fluorescence quantum yield in CD2Cl2. This implies that the ultrafast non-radiative deactivation is not simply a consequence of the small S(sub-1)-S(sub-0) energy gaps to the beta-meso-beta-fused porphyrin oligomers but with slower rates of S(sub-1)-S(sub-0) decay.

The Synthesis and Characterization of Highly Conjugated Oligomers Containing Ethyne-bridged Zinc Porphyrins

The Synthesis and Characterization of Highly Conjugated Oligomers Containing Ethyne-bridged Zinc Porphyrins PDF Author: Leahann N. Lapinski
Publisher:
ISBN:
Category :
Languages : en
Pages : 34

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