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4th EucheMs chemistry congress

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Poster Session 2<br />

s1185<br />

chem. Listy 106, s257–s1425 (2012)<br />

Poster session 2 - Green Chemistry<br />

P - 0 6 4 6<br />

SyntheSiS of SuCCiniC ACid derivAtiveS<br />

under MiCrowAve irrAdiAtion<br />

y. J. KiM 1 , J. h. SonG 2<br />

1 Chungnam National University, Chemistry, Daejeon, Republic<br />

of Korea<br />

2 Sunchon National University, Chemistry, Sunchon, Republic of<br />

Korea<br />

Dioctyl succinates and succinic anhydride were synthesized<br />

from succinic acid in the presence of a cation exchange resin,<br />

Amberlite IR-120. The synthesis of dioctyl succinate from<br />

succinic acid and octanol was perfomed in 18 h reflux condition<br />

with Amberlite IR-120 and the isolated yield of product was over<br />

90 %. For the synthesis of succinic anhydride, succinic acid was<br />

refluxed in isopropenyl acetate for 18 h with Amberlite IR-120 as<br />

a catalyst. The long reaction time was significantly reduced to less<br />

than 10 min under microwave irradiation. We will discuss the<br />

chemical transformation using microwave irradiation method and<br />

the reusability of catalyst.<br />

Keywords: Catalyst Reuseability; Microwave Irradiation;<br />

4 th <strong>EucheMs</strong> <strong>chemistry</strong> <strong>congress</strong><br />

P - 0 6 4 7<br />

wAter-SoLuBLe tin(iv) PorPhyrinS AS<br />

PhotoSenSitiSerS for ArtifiCiAL<br />

PhotoSyntheSiS<br />

A. M. MAnKe 1 , P. Kurz 1 , K. GeiSeL 2<br />

1 Institut für Anorg. Chemie, Christian-Albrechts-Universität,<br />

Kiel, Germany<br />

2 Institut für Phys. Chem., RWTH Aachen Universität, Aachen,<br />

Germany<br />

Light-driven water-splitting into hydrogen and oxygen is a<br />

concept for sustainable energy generation. This concept is inspired<br />

by basic principles of photosynthesis, the process where solar<br />

energy is converted into chemically stored energy in nature.<br />

In vivo, chlorophyll molecules act as light absorbing molecules<br />

and electron transfer agents. They generate both the high oxidising<br />

potentials for water-oxidation and the strong reducing agents for<br />

NADP + -reduction.<br />

We study the water-soluble tin(IV) porphyrins dichlorido-<br />

-5,10,15,20-tetrakis(p-carboxyphenyl)-porphyrinato-tin(IV)<br />

(SnTPPC) and dichlorido-5,10,15,20-tetrakis(p-sulfophenyl)-<br />

-porphyrinato-tin(IV) (SnTPPS) as possible mimics for<br />

chlorophyll dyes. The compounds show favourable redox<br />

potentials to act as photosensitisers in an artificial system for<br />

light-driven water-splitting. We tested the ability of these synthetic<br />

porphyrins to act as photosensitisers in photocatalytic model<br />

systems and especially detected promising rates for light-induced<br />

H formation in a photocatalytic system developed by Krüger and<br />

2<br />

Fuhrhop. [1] Details on possible mechanisms, the reaction kinetics,<br />

photosensitiser stability and the use of different electron donors<br />

will be presented.<br />

references:<br />

1. W. Krüger, J. H. Fuhrhop, Angew. Chem. Int. Ed. 21, 131<br />

(1982).<br />

Keywords: Bioinorganic <strong>chemistry</strong>; energy conversion;<br />

homogeneous catalysis; porphyrinoids; water splitting;<br />

AUGUst 26–30, 2012, PrAGUE, cZEcH rEPUbLIc

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