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1 Obsah<br />

1 OBSAH ......................................................................................................................... 1<br />

2 ÚVOD ............................................................................................................................ 3<br />

3 TEORETICKÁ ČÁST ................................................................................................. 4<br />

3.1 KOORDINAČNÍ CHEMIE A KOORDINAČNÍ SLOUČENINY ............................................ 4<br />

3.2 KOORDINAČNÍ SLOUČENINY MĚDI ........................................................................... 5<br />

3.2.1 Chemická charakteristika mědi a její role v biologických procesech ............... 5<br />

3.2.2 Měď z pohledu koordinační chemie ................................................................... 8<br />

3.2.3 Biologicky aktivní koordinační sloučeniny mědi ............................................... 9<br />

3.2.4 Fyziologické účinky koordinačních sloučenin mědi ........................................ 20<br />

4 EXPERIMENTÁLNÍ ČÁST ..................................................................................... 29<br />

4.1 POUŽÍVANÉ PŘÍSTROJE .......................................................................................... 29<br />

4.2 SYNTÉZA (2–FENYL)–3–HYDROXY–4(1H)–CHINOLONŮ....................................... 29<br />

4.2.1 BROMACE ACETOFENONU ......................................................................... 29<br />

4.2.2 ESTERIFIKACE ............................................................................................... 30<br />

4.2.3 CYKLIZACE ..................................................................................................... 30<br />

4.3 PŘÍPRAVY JEDNOTLIVÝCH CHINOLONŮ .................................................. 31<br />

4.3.1 2–fenyl–3–hydroxy–4(1H)–chinolon (Q1)....................................................... 32<br />

4.3.2 2–(4–methyl)fenyl–3–hydroxy–4(1H)–chinolon (Q2) ..................................... 32<br />

4.3.3 2–(4–methoxy)fenyl–3–hydroxy–4(1H)–chinolon (Q3)................................... 33<br />

4.3.4 2–(4–fluoro)fenyl–3–hydroxy–4(1H)–chinolon (Q4) ...................................... 33<br />

4.3.5 2–(4–chlor)fenyl–3–hydroxy–4(1H)–chinolon (5) .......................................... 33<br />

4.3.6 2–(4–amino–3,5–dichloro)fenyl–3–hydroxy–4(1H)–chinolon (Q6) ............... 34<br />

4.4 SYNTÉZA KOORDINAČNÍCH SLOUČENIN MĚDI A 2–FENYL–3–<br />

HYDROXY–4(1H)–CHINOLONOVÝCH DERIVÁTŮ................................................ 34<br />

5 VÝSLEDKY A DISKUZE ........................................................................................ 36<br />

5.1 FYZIKÁLNĚ CHEMICKÁ CHARAKTERISTIKA PŘIPRAVENÝCH KOMPLEXŮ MĚDI ....... 37<br />

5.1.1 Bis–[3–(hydroxy–O)–2–fenyl–4(1H)–chinolinonato–O 4 ]měďnatý komplex<br />

(1) 37<br />

5.1.2 Bis–[3–(hydroxy–O)–2–(4–methyl)fenyl–4(1H)–chinolinonato–O 4 ]měďnatý<br />

komplex (2) .................................................................................................................. 38<br />

5.1.3 Bis–[3–(hydroxy–O)–2–(4–methoxy)fenyl–4(1H)–chinolinonato–<br />

O 4 ]měďnatý komplex (3)............................................................................................ 38<br />

5.1.4 Bis–[3–(hydroxy–O)–2–(4–fluoro)fenyl–4(1H)–chinolinonato–O 4 ]měďnatý<br />

komplex (4) .................................................................................................................. 39<br />

5.1.5 Bis–[3–(hydroxy–O)–2–(chloro)fenyl–4(1H)–chinolinonato–O 4 ]měďnatý<br />

komplex (5) .................................................................................................................. 40<br />

5.1.6 Bis–[3–(hydroxy–O)–2–(4,6–dichloro–5–amino)fenyl–4(1H)–chinolinonato–<br />

O 4 ]měďnatý komplex (6)............................................................................................ 41<br />

5.2 STANOVENÍ ANTIMIKROBIÁLNÍ AKTIVITY ............................................................. 42<br />

6 ZÁVĚR ....................................................................................................................... 45<br />

7 LITERATURA ........................................................................................................... 46<br />

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