Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat:
Gespeichert in:
| 1. Verfasser: | |
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| Format: | Abschlussarbeit Buch |
| Sprache: | German |
| Veröffentlicht: |
Berlin
Mensch und Buch Verlag
[2019]
|
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis Inhaltsverzeichnis |
| Beschreibung: | VI, 263 Seiten Illustrationen, Diagramme 21 cm |
| ISBN: | 9783863879570 |
Internformat
MARC
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| 016 | 7 | |a 1180434161 |2 DE-101 | |
| 020 | |a 9783863879570 |c Broschur |9 978-3-86387-957-0 | ||
| 035 | |a (OCoLC)1136406350 | ||
| 035 | |a (DE-599)DNB1180434161 | ||
| 040 | |a DE-604 |b ger |e rda | ||
| 041 | 0 | |a ger | |
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| 049 | |a DE-29T | ||
| 082 | 0 | |a 547.05 |2 23/ger | |
| 084 | |a 540 |2 sdnb | ||
| 100 | 1 | |a Baars, Sania |d 1982- |e Verfasser |0 (DE-588)1180414640 |4 aut | |
| 245 | 1 | 0 | |a Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat |c vorgelegt von Dipl. Chem. Sania Baars geb. Daova |
| 264 | 1 | |a Berlin |b Mensch und Buch Verlag |c [2019] | |
| 300 | |a VI, 263 Seiten |b Illustrationen, Diagramme |c 21 cm | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 502 | |b Dissertation |c Rheinische Friedrich-Wilhelms-Universität Bonn |d 2019 | ||
| 650 | 0 | 7 | |a Chemische Synthese |0 (DE-588)4133806-6 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Cyclopentadienylion |0 (DE-588)4336321-0 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Trifluormethylgruppe |0 (DE-588)4186117-6 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Metallorganische Chemie |0 (DE-588)4602390-2 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Kation |0 (DE-588)4163478-0 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Ligand |0 (DE-588)4035711-9 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Reaktivität |0 (DE-588)4208182-8 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Sulfonate |0 (DE-588)4184048-3 |2 gnd |9 rswk-swf |
| 655 | 7 | |0 (DE-588)4113937-9 |a Hochschulschrift |2 gnd-content | |
| 689 | 0 | 0 | |a Sulfonate |0 (DE-588)4184048-3 |D s |
| 689 | 0 | 1 | |a Trifluormethylgruppe |0 (DE-588)4186117-6 |D s |
| 689 | 0 | 2 | |a Cyclopentadienylion |0 (DE-588)4336321-0 |D s |
| 689 | 0 | 3 | |a Kation |0 (DE-588)4163478-0 |D s |
| 689 | 0 | 4 | |a Chemische Synthese |0 (DE-588)4133806-6 |D s |
| 689 | 0 | |5 DE-604 | |
| 689 | 1 | 0 | |a Sulfonate |0 (DE-588)4184048-3 |D s |
| 689 | 1 | 1 | |a Trifluormethylgruppe |0 (DE-588)4186117-6 |D s |
| 689 | 1 | 2 | |a Cyclopentadienylion |0 (DE-588)4336321-0 |D s |
| 689 | 1 | 3 | |a Ligand |0 (DE-588)4035711-9 |D s |
| 689 | 1 | 4 | |a Reaktivität |0 (DE-588)4208182-8 |D s |
| 689 | 1 | 5 | |a Metallorganische Chemie |0 (DE-588)4602390-2 |D s |
| 689 | 1 | |5 DE-604 | |
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| 856 | 4 | 2 | |m DNB Datenaustausch |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=031706541&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-031706541 | ||
Datensatz im Suchindex
| _version_ | 1804180819473858560 |
|---|---|
| adam_text | INHALTSVERZEICHNIS
INHALTSVERZEICHNIS
........................................................................................................................
III
1
EINLEITUNG
.............................................................................................................................
1
1.1
HISTORISCHER
RUECKBLICK
IN
DIE
ENTWICKLUNG
DER
AROMATIZITAET
UND
DER
ANTIAROMATIZITAET...
1
1.2
KRITERIEN
FUER
AROMATIZITAET
UND
ANTIAROMATIZITAET
................................................................
6
1.3
CYCLOPENTADIENYL
KATIONEN
ALS
ANTIAROMATISCHE
MODELSYSTEME
UND
DEREN
EXPERIMENTELLE
NACHWEISE
...............................................................................................
8
1.4
PENTAKIS(DIMETHYLAMINO)CYCLOPENTADIENYLIUM
TRIFLUORMETHANSULFONAT
.......................
14
1.5
DIE
ROLLE
VON
COBALT(L)
IN
DER
CYCLOTRIMERISATION
.........................................................
22
2
ZIELSETZUNG
..........................................................................................................................
28
3
ERGEBNISSE
UND
DISKUSSION
................................................................................................
30
3.1
SYNTHESE
UND
CHARAKTERISIERUNG
VON
PENTAKIS(DIMETHYLAMINO)CYCLOPENTADIENYLIUM
T
RIFLUORMETHYLSULFONAT
.....................................................................................................
30
3.2
REAKTIVITAET
VON
PENTAKIS(DIMETHYLAMINO)CYCLOPENTADIENYLIUM
TRIFLUROMETHYLSULFONAT
46
3.2.1
REAKTIVITAET
GEGENUEBER
CARBONYL-METALLATEN
..........................................................46
3.2.2
RINGERWEITERUNGSREAKTION
......................................................................................
63
3.2.3
REAKTIVITAET
GEGENUEBER
FUNKTIONALISIERTEN
ALKINEN
.................................................
67
3.2.4
REAKTIVITAET
GEGENUEBER
REDUKTIONSMITTELN
.............................................................
71
3.3
C-C-KUPPLUNGSCHEMIE
AM
[CO{/7
5
-C
5
(NME
2
)5}(CO)2]
(18)
............................................
82
3.3.1
SYNTHESE
DES
COBALTACYCLOBUTENONS
24
...............................................................
83
3.3.2
REAKTIVITAET
DES
COBALTACYCLOBUTANONS
GEGENUEBER
ISONITRILEN
..............................
90
3.3.3
DECARBONYLIERUNG
DES
COBALATACYCLOBUTENONS
24
.............................................
101
3.4
NUCLEOPHILE
EIGENSCHAFTEN
VON
PENTAKIS(DIMETHYLAMINO)PYRIDIN
..............................
113
3.4.1
REAKTIVITAET
VON
21
GEGENUEBER
H
+
.........................................................................
115
3.4.2
REAKTIVITAET
VON
21
GEGENUEBER
ME
+
.......................................................................
125
3.4.3
REAKTIVITAET
VON
21
GEGENUEBER
ELEKTROPHILEN
DER
GRUPPE
14..............................
127
3.4.4
REAKTIVITAET
VON
21
GEGENUEBER
OXIDATIONSMITTELN
................................................
136
3.5
KOORDINATIONSCHEMIE
VON
LI[C
5
(NME
2
)5]
(3-A)
.............................................................
143
3.6
REAKTIVITAETSUNTERSUCHUNGEN
AN
DEM
IMIN
XLLL-ME
......................................................
154
4
ZUSAMMENFASSUNG
UND
AUSBLICK
......................................................................................
163
4.1
ZUSAMMENFASSUNG
.......................................................................................................
163
4.2
AUSBLICK
.........................................................................................................................
178
5
EXPERIMENTELLER
TEIL
...........................................................................................................
182
5.1
ALLGEMEINE
ARBEITSTECHNIKEN
.......................................................................................
182
5.2
ANALYTISCHE
METHODEN
..................................................................................................
184
5.2.1
KERNSPINRESONANZSPEKTROSKOPIE
.........................................................................
184
IV
5.2.2
ELEMENTARANALYSEN
..............................................................................................
185
5.2.3
SCHMELZPUNKTBESTIMMUNG
...................................................................................
185
5.2.4
ROENTGENBEUGUNG
AN
EINKRISTALLEN
........................................................................
185
5.2.5
INFRAROTSPEKTROSKOPIE
............................................................................................
186
5.2.6
UV/VIS-SPEKTROSKOPIE
..........................................................................................
186
5.2.7
CYCLOVOLTAMETRISCHE
MESSUNGEN
.........................................................................
187
5.2.8
MAGNETISCHE
MESSUNGEN
.....................................................................................
187
5.3
SYNTHESEN
LITERATURBEKANNTER
VERBINDUNGEN
..............................................................
188
5.4
KOMMERZIELL
ERWORBENE
SUBSTANZEN
...........................................................................
189
5.5
SYNTHESEN
......................................................................................................................
189
5.5.1
METHYLIMINO-TETRAKIS(DIMETHYLAMINO)CYCLOPENTADIEN
(XLLL-ME)
............................
189
5.5.2
PENTAKIS(DIMETHYLAMINO)CYCLOPENTADIENYLIUM-TRIFLUORMETHYLSULFONAT
(1
-OTF)
...
190
5.5.3
PENTAKIS(DIMETHYLAMINO)CYCLOPENTADIEN
(2)
.......................................................
192
5.5.4
LI[C
5
(NME
2
)
5
]
(3-A)
...............................................................................................
192
5.5.5
[TA{/7
5
-C
5
(NME
2
)5}(CO)4]
(12)
...............................................................................
194
5.5.6
[MN{/7
5
-C5(NME
2
)5}(CO)
3
]
(15)
..............................................................................
196
5.5.7
[CO{/7
5
-C
5
(NME
2
)
5
}(CO)
2
]
(18)
..............................................................................
197
5.5.8
[FE{/)
5
-C
5
(NME
2
)
5
}(CO)
2
]
2
(19)
.............................................................................
198
5.5.9
[C
5
H
2
(NME
2
)
5
]CI
(20-CI)
.......................................................................................
199
5.5.10
NC
5
(NME
2
)
5
(21)
...................................................................................................200
5.5.11
[C
5
(NME
2
)4{=C(NME
2
)C(NME
2
)
2
}]OTF
(22)
...........................................................
201
5.5.12
[CO{/7
5
-C
5
(NME
2
)
5
}(CO)LM-ME
4
]
(23)
................................................................... 202
5.5.13
[CO{R)
5
-C
5
(NME
2
)5}{K
2
-C
3
(NME
2
)
2
(O)}]
(24)
..........................................................203
5.5.14
[CO{/7
5
-C
5
(NME
2
)
5
}(/C
2
-C(NME)C(NME
2
)C(NME
2
)C(O)C(NME))]
(26)
................. 204
5.5.15
[CO{N
5
-C
5
(NME
2
)
5
}(/
2
-C3(NME
2
)
2
(O)}(CN BU)]
(27)
.............................................205
5.5.16
UMSETZUNG
VON
K[CO(CO)
4
]
MIT
TRIS(DIMETHYLAMINO)CYCLOPROPINIUM-CHLORID
...205
5.5.17
PHOTOLYSE
VON
[C
3
(NME
2
)3][CO(CO)4]
(XXIII-2)
...................................................
206
5.5.18
[CO{/7
5
-C
5
(NME
2
)
5
}(/?
2
-ME
2
NC2CNME
2
)]
(30)
.......................................................206
5.5.19
[CO{/7
5
-C
5
(NME
2
)5}{/7
3
-(=C(NME
2
)C(H)NME
2
)}][B(3,5-(CF3)
2
-C
6
H
3
)4](31)
..........208
5.5.20
[CO{/7
5
-C
5
(NME
2
)
5
}{/
2
-C
3
(NME
2
)
2
(=N
!
BU3)}]
(32)
................................................. 208
5.5.21
PROTONIERUNG
VON
21
MIT
[H(ET
2
O)
2
][B(C
6
H3-3,5-(CF
3
)
2
)
4
]
(XXV)
......................... 209
5.5.22
[NC
5
H(NME
2
)5][B(3,5-(CF3)
2
-C
6
H3)4]
(34-3)
.........................................................
211
5.5.23
[NC
5
(NME3)(NME
2
)
4
][BF
4
]
(35)
.............................................................................212
5.5.24
CI
2
GE
NC
5
(NME
2
)
5
(36)
........................................................................................213
5.5.25
[NC
5
{(NME
2
)
2
GECI}(NME
2
)3][GECL3]
(37)
.............................................................213
5.5.26
CI
2
SN
NC
5
(NME
2
)
5
(38)
.........................................................................................215
V
5.5.27
[NC
5
(NME
2
)
5
][PF
6
]
2
(39)
.......................................................................................
216
5.5.28
[NK^-CSTNMEZHD
(40)
.......................................................................................
217
5.5.29
[CO{Z)
5
-C
5
(NME
2
)
5
}BR]
2
(41)
..................................................................................217
5.5.30
[CO{/)
5
-C5(NME
2
)5}(0
5
-C
5
H5)]
(42)
.........................................................................
218
5.5.31
UMSETZUNG
VON
LI[C
5
(NME
2
)5]
MIT
FEBR
2
BEI
RAUMTEMPERATUR
..........................218
5.5.32
UMSETZUNG
VON
LI[C
5
(NME
2
)
5
]
MIT
FEBR
2
BEI
TIEFEN
TEMPERATUREN
.....................219
5.5.33
[MO{/C
2
-C
5
(NME
2
)4(NME)}(CO)
4
]
(44)
...................................................................219
5.5.34
[GE(CI)
2
{K
1
-C
5
(NME
2
)
4
(NME)}]
(45)
.....................................................................
220
6
ANHANG
............................................................................................................................
222
6.1
KRISTALLOGRAPHISCHE
DATEN
SOWIE
PARAMETER
DER
MESSUNGEN
UND
STRUKTURVERFEINERUNGEN
........................................................................................................222
6.1.1
LI[C
5
(NME
2
)
5
]
(3-A)
...............................................................................................222
6.1.2
[C
5
H(NME
2
)
4
(N=ME)]OTF
(9)
................................................................................
222
6.1.3
[C
5
(NME
2
)3(H)(NME)(CH
2
NME
2
)]OTF
(10)
...........................................................
223
6.1.4
[C
5
(NME
2
)
5
]
2
[FEBR
4
]
(11)
.....................................................................................
224
6.1.5
[TA(/7
5
-C
5
(NME
2
)
5
}(CO)
4
]
(12)
...............................................................................
224
6.1.6
[TA{//
5
-C
5
H(NME
2
)
4
}(CO)
4
]
(13)
............................................................................225
6.1.7
[MN{/?
5
-C
5
(NME
2
)
5
}(CO)
3
]
(15)
..............................................................................225
6.1.8
[MN{/7
5
-C
5
H(NME
2
)
4
}(CO)
3
]
(16)
...........................................................................226
6.1.9
[CO{R)
5
-C
5
(NME
2
)
5
}(CO)
2
]
(18)
..............................................................................
227
6.1.10
[H
2
C
5
(NME
2
)
5
]CI
(20)
............................................................................................227
6.1.11
[NC
5
(NME
2
)
5
]
(21)
.................................................................................................228
6.1.12
[NC
5
[C
5
(NME
2
)
4
{=C(NME
2
)C(NME
2
)
2
}]OTF
(22)
.................................................229
6.1.13
[CO{O
5
-C
5
(NME
2
)5}(CO)(LMME
4
)]
(23)
..................................................................229
6.1.14
[CO{R)
5
-C
5
(NME
2
)
5
}{K
2
-C
3
(NME
2
)
2
(O)}]
(24)
......................................................... 230
6.1.15
[CO{/7
5
-C
5
(NME
2
)
5
}{/
2
-C
3
(NME
2
)
2
(O)}{CN BU}]
(26)
.............................................
231
6.1.16
[CO{/7
5
-C
5
(NME
2
)
5
}(/
2
-C(NME)C(NME
2
)C(NME
2
)C(O)C(NME))](27)
.................
231
6.1.17
[CO{R?
3
-C
4
(NME
2
)
3
(O)}(CO)
3
]
(28)
........................................................................
232
6.1.18
[CO{C
3
(NME
2
)
3
}(CO)
2
]
2
(29)
................................................................................232
6.1.19
[CO{R)
5
-C
5
(NME
2
)
5
}(ME
2
NC=CNME
2
)]
(30)
...........................................................
233
6.1.20
[CO{/7
5
-C5(NME
2
)5}{0
3
-(=C(NME
2
)C(H)NME
2
)}][B(3,5-(CF
3
)
2
-C
6
H
3
)
4
]
(31)
..........234
6.1.21
[CO{/)
5
-C
5
H
5
}{/
2
-C
3
(NME
2
)
2
(=N BU
3
)}]
(32)
..........................................................234
6.1.22
[1-HNC
5
(NME
2
)
5
][B(3,5-(CF
3
)
2
-C
6
H
3
)
4
]
(34-1)
..................................................... 235
6.1.23
[2-NC
5
(HNME
2
)(NME
2
)
4
][B(3,5-(CF
3
)
2
-C
6
H
3
)
4
]
(34-2-N)
..................................... 236
6.1.24
[3-NC
5
(H)(NME
2
)5][B(3,5-(CF
3
)
2
-C
6
H
3
)
4
]
(34-3)
..................................................
236
6.1.25
[2-NC
5
(MENME
2
)(NME
2
)
4
][BF
4
]
(35)
.................................................................... 237
6.1.26
[NC
5
(NME
2
)
5
GECI][GECI
3
]
(37)
...........................................................................
237
VI
6.1.27
CI
2
SNNC
5
(NME
2
)
5
(38)
.........................................................................................238
6.1.28
[NC
5
(NME
2
)
5
][PF
6
]
2
(39)
........................................................................................239
6.1.29
[NI{F)
5
-C
5
(NME
2
)5}2]
(40)
........................................................................................239
6.1.30
[COBR{/7
5
-C
5
(NME
2
)
5
}]
2
(41)
..................................................................................240
6.1.31
[CO{O
5
-C
5
(NME
2
)
5
}(/7
5
-C
5
H
5
)]
(42)
.........................................................................
241
6.1.32
[FE{O
5
-C
5
(NME
2
)
5
}
2
]
(43)
.......................................................................................
241
6.1.33
[MO{/C
2
-C5(NME
2
)4(NME)}(CO)
4
]
(44)
.....................................................................
242
6.1.34
[GECI
2
{C
5
(NME
2
)
4
(NME)}]
(45)
.............................................................................
242
6.2
LISTE
ISOLIERTER
VERBINDUNGEN
........................................................................................244
6.3
ABKUERZUNGSVERZEICHNIS
................................................................................................
251
6.4
ABBILDUNGSVERZEICHNIS
.................................................................................................
253
6.5
SCHEMATAVERZEICHNIS
...................................................................................................
258
6.6
TABELLENVERZEICHNIS
......................................................................................................
260
6.7
WISSENSCHAFTLICHE
VEROEFFENTLICHUNGEN
.........................................................................
261
6.7.1
POSTERBEITRAEGE
AUF
WISSENSCHAFTLICHEN
KONFERENZEN
.........................................
261
6.7.2
OEFFENTLICHE
VORTRAEGE
.............................................................................................
261
6.8
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| any_adam_object | 1 |
| author | Baars, Sania 1982- |
| author_GND | (DE-588)1180414640 |
| author_facet | Baars, Sania 1982- |
| author_role | aut |
| author_sort | Baars, Sania 1982- |
| author_variant | s b sb |
| building | Verbundindex |
| bvnumber | BV046329661 |
| ctrlnum | (OCoLC)1136406350 (DE-599)DNB1180434161 |
| dewey-full | 547.05 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547.05 |
| dewey-search | 547.05 |
| dewey-sort | 3547.05 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie |
| format | Thesis Book |
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| genre | (DE-588)4113937-9 Hochschulschrift gnd-content |
| genre_facet | Hochschulschrift |
| id | DE-604.BV046329661 |
| illustrated | Illustrated |
| indexdate | 2024-07-10T08:41:49Z |
| institution | BVB |
| isbn | 9783863879570 |
| language | German |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-031706541 |
| oclc_num | 1136406350 |
| open_access_boolean | |
| owner | DE-29T |
| owner_facet | DE-29T |
| physical | VI, 263 Seiten Illustrationen, Diagramme 21 cm |
| publishDate | 2019 |
| publishDateSearch | 2019 |
| publishDateSort | 2019 |
| publisher | Mensch und Buch Verlag |
| record_format | marc |
| spelling | Baars, Sania 1982- Verfasser (DE-588)1180414640 aut Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat vorgelegt von Dipl. Chem. Sania Baars geb. Daova Berlin Mensch und Buch Verlag [2019] VI, 263 Seiten Illustrationen, Diagramme 21 cm txt rdacontent n rdamedia nc rdacarrier Dissertation Rheinische Friedrich-Wilhelms-Universität Bonn 2019 Chemische Synthese (DE-588)4133806-6 gnd rswk-swf Cyclopentadienylion (DE-588)4336321-0 gnd rswk-swf Trifluormethylgruppe (DE-588)4186117-6 gnd rswk-swf Metallorganische Chemie (DE-588)4602390-2 gnd rswk-swf Kation (DE-588)4163478-0 gnd rswk-swf Ligand (DE-588)4035711-9 gnd rswk-swf Reaktivität (DE-588)4208182-8 gnd rswk-swf Sulfonate (DE-588)4184048-3 gnd rswk-swf (DE-588)4113937-9 Hochschulschrift gnd-content Sulfonate (DE-588)4184048-3 s Trifluormethylgruppe (DE-588)4186117-6 s Cyclopentadienylion (DE-588)4336321-0 s Kation (DE-588)4163478-0 s Chemische Synthese (DE-588)4133806-6 s DE-604 Ligand (DE-588)4035711-9 s Reaktivität (DE-588)4208182-8 s Metallorganische Chemie (DE-588)4602390-2 s B:DE-101 application/pdf http://d-nb.info/1180434161/04 Inhaltsverzeichnis DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=031706541&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Baars, Sania 1982- Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat Chemische Synthese (DE-588)4133806-6 gnd Cyclopentadienylion (DE-588)4336321-0 gnd Trifluormethylgruppe (DE-588)4186117-6 gnd Metallorganische Chemie (DE-588)4602390-2 gnd Kation (DE-588)4163478-0 gnd Ligand (DE-588)4035711-9 gnd Reaktivität (DE-588)4208182-8 gnd Sulfonate (DE-588)4184048-3 gnd |
| subject_GND | (DE-588)4133806-6 (DE-588)4336321-0 (DE-588)4186117-6 (DE-588)4602390-2 (DE-588)4163478-0 (DE-588)4035711-9 (DE-588)4208182-8 (DE-588)4184048-3 (DE-588)4113937-9 |
| title | Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat |
| title_auth | Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat |
| title_exact_search | Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat |
| title_full | Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat vorgelegt von Dipl. Chem. Sania Baars geb. Daova |
| title_fullStr | Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat vorgelegt von Dipl. Chem. Sania Baars geb. Daova |
| title_full_unstemmed | Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat vorgelegt von Dipl. Chem. Sania Baars geb. Daova |
| title_short | Reaktivitätsstudien an dem elektronenreichen Pentakis(dimethylamino)cyclopentadienylium Trifluormethylsulfonat |
| title_sort | reaktivitatsstudien an dem elektronenreichen pentakis dimethylamino cyclopentadienylium trifluormethylsulfonat |
| topic | Chemische Synthese (DE-588)4133806-6 gnd Cyclopentadienylion (DE-588)4336321-0 gnd Trifluormethylgruppe (DE-588)4186117-6 gnd Metallorganische Chemie (DE-588)4602390-2 gnd Kation (DE-588)4163478-0 gnd Ligand (DE-588)4035711-9 gnd Reaktivität (DE-588)4208182-8 gnd Sulfonate (DE-588)4184048-3 gnd |
| topic_facet | Chemische Synthese Cyclopentadienylion Trifluormethylgruppe Metallorganische Chemie Kation Ligand Reaktivität Sulfonate Hochschulschrift |
| url | http://d-nb.info/1180434161/04 http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=031706541&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT baarssania reaktivitatsstudienandemelektronenreichenpentakisdimethylaminocyclopentadienyliumtrifluormethylsulfonat |
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