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Tabel 7.pdf - Ordbogen.com

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<strong>Tabel</strong> 7<br />

<strong>Tabel</strong> 7. Udvalgte cykliske stamhydrider med to eller flere heteroatomer<br />

1) 2)<br />

<strong>Tabel</strong> 7<br />

N<br />

N<br />

NH<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

N<br />

O<br />

N<br />

O<br />

N<br />

S<br />

N<br />

S<br />

pyrazol<br />

1H-1,2-diazol<br />

pyrazolidin<br />

1,2-diazolidin<br />

imidazol<br />

1H-1,3-diazol<br />

imidazolidin<br />

1,3-diazolidin<br />

H H H<br />

H<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

3H-pyrazol<br />

3H-1,2-diazol<br />

isoxazol<br />

1,2-oxazol<br />

1,3-oxazol<br />

isothiazol<br />

1,2-thiazol<br />

thiazol<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

N<br />

N<br />

NH<br />

N<br />

N<br />

N<br />

NH<br />

N<br />

N<br />

O<br />

N<br />

N<br />

N<br />

O<br />

O<br />

O<br />

O<br />

O<br />

O<br />

N<br />

O<br />

N<br />

S<br />

N<br />

Se<br />

S<br />

O<br />

H<br />

1<br />

2<br />

3<br />

4<br />

5<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1,2,5-oxadiazol pyridazin 1,2-diazinan pyrimidin 1,3-diazinan<br />

1,3-diazin<br />

1,2-diazin<br />

N<br />

N<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

H<br />

H<br />

H<br />

H<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

pyrazin<br />

1,4-diazin<br />

piperazin<br />

1,4-diazinan<br />

1,4-dioxin 1,4-dioxan 1,3-dioxan<br />

N<br />

O<br />

H H H H<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

4H-1,4-oxazin<br />

morpholin<br />

1,4-oxazinan<br />

thiomorpholin<br />

1,4-thiazinan<br />

selenomorpholin<br />

1,4-selenazinan<br />

1,4-oxathian<br />

oxazol<br />

1,3-thiazol


<strong>Tabel</strong> 7<br />

1<br />

6 O 2<br />

HB BH<br />

5 3<br />

O O<br />

B<br />

4<br />

H<br />

boroxin<br />

1,3,5,2,4,6-trioxatriborinan<br />

cyclotriboroxan<br />

1<br />

6 S 2<br />

HB BH<br />

5 3<br />

S 4 S<br />

B<br />

H<br />

borthiin<br />

1,3,5,2,4,6-trithiatriborinan<br />

cyclotriborathian<br />

H<br />

6 N 2<br />

HB 1 BH<br />

5 3<br />

HN NH<br />

B<br />

4<br />

H<br />

borazin<br />

1,3,5,2,4,6-triazatriborinan<br />

cyclotriborazan<br />

6<br />

5<br />

7<br />

1<br />

N<br />

2<br />

N<br />

5<br />

4<br />

3<br />

6<br />

indazol (her 3H-) benzimidazol (her 1H-) benzotriazol (her 1H-)<br />

H<br />

N<br />

N<br />

H<br />

N<br />

7 7<br />

1<br />

1<br />

6<br />

2<br />

2<br />

3<br />

5<br />

3<br />

4<br />

4<br />

N<br />

N<br />

7<br />

6<br />

8<br />

1<br />

2<br />

3<br />

5 4<br />

N<br />

N<br />

N<br />

7<br />

8<br />

cinnolin quinazolin quinoxalin<br />

1<br />

6<br />

3<br />

5 4<br />

N<br />

8<br />

2<br />

7<br />

6<br />

5<br />

1<br />

N<br />

N<br />

2<br />

4 3<br />

7<br />

6<br />

8 1<br />

2<br />

3<br />

N<br />

N<br />

5 4<br />

5 4<br />

7<br />

6<br />

8<br />

N<br />

1<br />

N<br />

2<br />

7<br />

3<br />

6<br />

phthalazin naphthyridin (her 1,8-) 3) naphthyridin (her 1,5-) 3)<br />

8<br />

5<br />

N<br />

1<br />

N<br />

4<br />

2<br />

3<br />

1<br />

2<br />

N<br />

N<br />

H<br />

N<br />

6 6<br />

8 1<br />

5 7<br />

7<br />

N<br />

N N<br />

1 5<br />

N<br />

7<br />

8<br />

8<br />

3 9<br />

2<br />

3<br />

3 9<br />

6 5<br />

4 N<br />

N<br />

4 N<br />

N<br />

4<br />

purin (her 7 H-) 4) purin (her 2 H-) 4) pteridin<br />

N<br />

2


<strong>Tabel</strong> 7<br />

9<br />

HN<br />

1<br />

2<br />

3<br />

N<br />

4<br />

9<br />

10<br />

N<br />

1<br />

N<br />

2<br />

3<br />

4<br />

8<br />

7<br />

5<br />

8<br />

5<br />

6<br />

7 6<br />

perimidin (her 1H-) phenanthrolin (her 1,10-) 3)<br />

9 1 9<br />

1<br />

9<br />

1<br />

O<br />

8 10<br />

2 8<br />

10<br />

2<br />

X<br />

8<br />

X<br />

10<br />

2<br />

7<br />

6<br />

5<br />

O<br />

4<br />

oxanthren<br />

X = S:<br />

dibenzo[1,4]dioxin 5) X = Se:<br />

X = Te:<br />

X = Hg:<br />

3<br />

7<br />

6<br />

5<br />

X<br />

4<br />

thianthren<br />

selenanthren<br />

telluranthren<br />

mercuranthren 6)<br />

3<br />

7<br />

6<br />

X<br />

X = N:<br />

X = P:<br />

X = As:<br />

X = SiH:<br />

X = B:<br />

5<br />

4<br />

3<br />

phenazin<br />

phosphanthren<br />

arsanthren<br />

silanthren<br />

boranthren<br />

8<br />

9 1<br />

9<br />

1<br />

X<br />

10<br />

2<br />

8<br />

X<br />

10<br />

2<br />

7<br />

6<br />

X = S:<br />

X = Se:<br />

X = Te:<br />

X = NH:<br />

X = PH:<br />

X = AsH:<br />

X = SbH:<br />

5<br />

3<br />

O<br />

4<br />

phenoxathiin<br />

phenoxaselenin<br />

phenoxatellurin<br />

phenoxazin (her 10H-)<br />

phenoxaphosphin 7)<br />

phenoxaphosphinin (her 10H-)<br />

phenoxarsin 7)<br />

phenoxarsinin (her 10H-)<br />

phenoxantimonin 7)<br />

phenoxastibinin (her 10H-)<br />

8<br />

7<br />

9<br />

X = Se, Z = NH:<br />

X = Se, Z = PH:<br />

X = Te, Z = NH:<br />

6<br />

X = Se:<br />

X = NH:<br />

X = PH:<br />

X = AsH:<br />

Z<br />

10<br />

5<br />

X<br />

7<br />

1<br />

4<br />

6<br />

S<br />

phenothiaselenin<br />

phenothiazin (her 10H-)<br />

phenothiaphosphinin (her 10H-)<br />

phenothiarsin 7)<br />

phenothiarsinin (her 10H-)<br />

2<br />

3<br />

phenoselenazin (her 10H-)<br />

phenoselenaphosphinin (her 10H-)<br />

phenotellurazin (her 10H-)<br />

5<br />

4<br />

3


<strong>Tabel</strong> 7<br />

8<br />

9<br />

X<br />

10<br />

1 9<br />

2<br />

8<br />

X<br />

10<br />

1<br />

2<br />

7<br />

6<br />

5<br />

N<br />

X = P: phenophosphazinin 8)<br />

X = As: phenarsazinin 8)<br />

X = Sb: phenazastibinin 8)<br />

4<br />

3<br />

7<br />

6<br />

X = As:<br />

X = Sb:<br />

5<br />

P<br />

phenophospharsinin 8)<br />

phenophosphastibinin 8)<br />

4<br />

3<br />

9<br />

8<br />

7<br />

Hg<br />

10<br />

5<br />

1<br />

2<br />

3<br />

2<br />

N<br />

N<br />

6<br />

H<br />

4<br />

H<br />

5H-phenomercurazin 9) azandiyldi-o-phenylenkviksølv 9)<br />

Hg<br />

1) De anførte navne er stamnavne ( 2.3), hvis ikke andet er bemærket. Se også tabel 14D: bilan, corrin, phthalocyanin,<br />

porphyrin, yohimban.<br />

2) Hvor samme navn dækker over flere tautomerer, er kun vist én eller to tautomerer og de tilhørende navne med indiceret<br />

hydrogen. Hvor samme navn anvendes om flere isomerer, der adskiller sig ved heteroatomers positioner, er kun vist én<br />

eller to isomerer og de tilhørende navne med eksplicitte heteroatomlokanter.<br />

3) Tilsvarende 1,6-; 1,7-; 2,6- og 2,7-naphthyridin og 1,7-; 1,8-; 1,9-; 2,7-; 2,8-; 2,9-; 3,7-; 3,8- og 4,7-phenanthrolin; alle<br />

med ét nitrogenatom i hver terminal ring. Nummereringen i phenanthrolinskelettet er forskellig fra nummereringen af<br />

den tilgrundliggende carbocykliske stamforbindelse, phenanthren (tabel 5).<br />

4) Ukonventionel nummerering.<br />

5) Fusionsnavn ( 2.3.5.2) ud fra Hantzsch-Widman-navnet 1,4-dioxin (se ovenfor i tabellen).<br />

6) Tidligere phenomercurin. Se også koordinationsnavnet foreslået i 3.9.2.2.<br />

7) Disse navne er foreslået i [3, s. 466-471] og i en tabel i [4, s. 170], men forladt i 1998 [8].<br />

8) Disse navne med gruppe 15-heteroatomaffikser er så vidt vides i overensstemmelse med 1998-reglerne [8]. Navnene<br />

phenophosphazinin og phenarsazinin er nævnt eksplicit, og det påpeges, at de bryder Hantzsch-Widman-rækkefølgen.<br />

9) Koordinationsnavnet kan ikke bruges som stamnavn, da der ikke er nogen oplagt nummerering.

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