Improving intramolecular hydroamination Rh(i) and Ir(i) catalysts through targeted ligand modificationCCDC reference numbers 291181 (6), 291475 (8), 291177 (9), 291474 (10), 729970 (11). For crystallographic data in CIF or other electronic format see DOI: 10.1039/b9nj00759h
A series of complexes containing the phosphino-pyrazolyl ligand 1-(2-(diphenylphosphino)phenyl)pyrazole (PyPhP) and 1-(2-(diphenylphosphino)ethyl)pyrazole (PyP) were synthesized: [Ir(PyPhP)(COD)]BPh 4 , [Ir(PyPhP)(CO) 2 ]BPh 4 , Rh(PyPhP)(CO)Cl and Ir(PyPhP)(CO)Cl. The complexes Rh(PyP)(CO)OSO 2 CF...
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| creator | Beeren, Sophie R Dabb, Serin L Edwards, Gavin Smith, Matthew K Willis, Anthony C Messerle, Barbara A |
| description | A series of complexes containing the phosphino-pyrazolyl ligand 1-(2-(diphenylphosphino)phenyl)pyrazole (PyPhP) and 1-(2-(diphenylphosphino)ethyl)pyrazole (PyP) were synthesized: [Ir(PyPhP)(COD)]BPh
4
, [Ir(PyPhP)(CO)
2
]BPh
4
, Rh(PyPhP)(CO)Cl and Ir(PyPhP)(CO)Cl. The complexes Rh(PyP)(CO)OSO
2
CF
3
and Rh(PyPhP)(CO)OSO
2
CF
3
were also synthesized, using the parent complexes Rh(PyP)(CO)Cl and Rh(PyPhP)(CO)Cl. The solid-state structures of the new complexes were determined by X-ray diffraction analysis. The cationic Ir(
i
) complex [Ir(PyPhP)(COD)]BPh
4
was found to be a highly efficient catalyst for the intramolecular hydroamination of 4-pentyn-1-amine, achieving a turnover rate of 1500 h
−1
, with >98% conversion in 6 minutes. The efficiency of the catalyzed hydroamination of 4-pentyn-1-amine using the neutral Ir(
i
) and Rh(
i
) complexes as catalysts was significantly improved by generating active catalysts
in situ
through abstraction of a chloride ligand by reaction with AgOSO
2
CF
3
, TMSOSO
2
CF
3
or NaBPh
4
. The catalytic efficiency of the catalysts generated from Ir(PyP)(CO)Cl and a sodium salt were found to be inversely proportional to the coordinating strength of the counter-ion of the sodium salt. Rh(PyP)(CO)OSO
2
CF
3
is a more efficient catalyst for the cyclization of 4-pentyn-1-amine than the complex generated
in situ
from AgOSO
2
CF
3
and chloride complex Rh(PyP)(CO)Cl indicating that the higher lability of the triflate co-ligand of Rh(PyP)(CO)OSO
2
CF
3
, compared to the chloride co-ligand of Rh(PyP)(CO)Cl, enhances the catalytic activity of the Rh(
i
) complexes.
Catalysed intramolecular hydroamination of 4-pentyn-1-amine was achieved with a turnover rate of 1500 h
−1
( >98% conversion in 6 minutes). Activation of catalysts
in situ
through chloride abstraction was also investigated. |
| doi_str_mv | 10.1039/b9nj00759h |
| format | Article |
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4
, [Ir(PyPhP)(CO)
2
]BPh
4
, Rh(PyPhP)(CO)Cl and Ir(PyPhP)(CO)Cl. The complexes Rh(PyP)(CO)OSO
2
CF
3
and Rh(PyPhP)(CO)OSO
2
CF
3
were also synthesized, using the parent complexes Rh(PyP)(CO)Cl and Rh(PyPhP)(CO)Cl. The solid-state structures of the new complexes were determined by X-ray diffraction analysis. The cationic Ir(
i
) complex [Ir(PyPhP)(COD)]BPh
4
was found to be a highly efficient catalyst for the intramolecular hydroamination of 4-pentyn-1-amine, achieving a turnover rate of 1500 h
−1
, with >98% conversion in 6 minutes. The efficiency of the catalyzed hydroamination of 4-pentyn-1-amine using the neutral Ir(
i
) and Rh(
i
) complexes as catalysts was significantly improved by generating active catalysts
in situ
through abstraction of a chloride ligand by reaction with AgOSO
2
CF
3
, TMSOSO
2
CF
3
or NaBPh
4
. The catalytic efficiency of the catalysts generated from Ir(PyP)(CO)Cl and a sodium salt were found to be inversely proportional to the coordinating strength of the counter-ion of the sodium salt. Rh(PyP)(CO)OSO
2
CF
3
is a more efficient catalyst for the cyclization of 4-pentyn-1-amine than the complex generated
in situ
from AgOSO
2
CF
3
and chloride complex Rh(PyP)(CO)Cl indicating that the higher lability of the triflate co-ligand of Rh(PyP)(CO)OSO
2
CF
3
, compared to the chloride co-ligand of Rh(PyP)(CO)Cl, enhances the catalytic activity of the Rh(
i
) complexes.
Catalysed intramolecular hydroamination of 4-pentyn-1-amine was achieved with a turnover rate of 1500 h
−1
( >98% conversion in 6 minutes). Activation of catalysts
in situ
through chloride abstraction was also investigated.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/b9nj00759h</identifier><language>eng</language><creationdate>2010-06</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Beeren, Sophie R</creatorcontrib><creatorcontrib>Dabb, Serin L</creatorcontrib><creatorcontrib>Edwards, Gavin</creatorcontrib><creatorcontrib>Smith, Matthew K</creatorcontrib><creatorcontrib>Willis, Anthony C</creatorcontrib><creatorcontrib>Messerle, Barbara A</creatorcontrib><title>Improving intramolecular hydroamination Rh(i) and Ir(i) catalysts through targeted ligand modificationCCDC reference numbers 291181 (6), 291475 (8), 291177 (9), 291474 (10), 729970 (11). For crystallographic data in CIF or other electronic format see DOI: 10.1039/b9nj00759h</title><description>A series of complexes containing the phosphino-pyrazolyl ligand 1-(2-(diphenylphosphino)phenyl)pyrazole (PyPhP) and 1-(2-(diphenylphosphino)ethyl)pyrazole (PyP) were synthesized: [Ir(PyPhP)(COD)]BPh
4
, [Ir(PyPhP)(CO)
2
]BPh
4
, Rh(PyPhP)(CO)Cl and Ir(PyPhP)(CO)Cl. The complexes Rh(PyP)(CO)OSO
2
CF
3
and Rh(PyPhP)(CO)OSO
2
CF
3
were also synthesized, using the parent complexes Rh(PyP)(CO)Cl and Rh(PyPhP)(CO)Cl. The solid-state structures of the new complexes were determined by X-ray diffraction analysis. The cationic Ir(
i
) complex [Ir(PyPhP)(COD)]BPh
4
was found to be a highly efficient catalyst for the intramolecular hydroamination of 4-pentyn-1-amine, achieving a turnover rate of 1500 h
−1
, with >98% conversion in 6 minutes. The efficiency of the catalyzed hydroamination of 4-pentyn-1-amine using the neutral Ir(
i
) and Rh(
i
) complexes as catalysts was significantly improved by generating active catalysts
in situ
through abstraction of a chloride ligand by reaction with AgOSO
2
CF
3
, TMSOSO
2
CF
3
or NaBPh
4
. The catalytic efficiency of the catalysts generated from Ir(PyP)(CO)Cl and a sodium salt were found to be inversely proportional to the coordinating strength of the counter-ion of the sodium salt. Rh(PyP)(CO)OSO
2
CF
3
is a more efficient catalyst for the cyclization of 4-pentyn-1-amine than the complex generated
in situ
from AgOSO
2
CF
3
and chloride complex Rh(PyP)(CO)Cl indicating that the higher lability of the triflate co-ligand of Rh(PyP)(CO)OSO
2
CF
3
, compared to the chloride co-ligand of Rh(PyP)(CO)Cl, enhances the catalytic activity of the Rh(
i
) complexes.
Catalysed intramolecular hydroamination of 4-pentyn-1-amine was achieved with a turnover rate of 1500 h
−1
( >98% conversion in 6 minutes). Activation of catalysts
in situ
through chloride abstraction was also investigated.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFUE1Lw0AQjaJg_bj0Loy3FGzdadJs12tqMSdBvJdtsklWkt0wuxX67936gQdBT_PevDfw3kTRGNkMWSLutsK8MsYXoj2ORphkYirmGZ4EjGk6ZYs0O4vOnQseRJ7h6Ghc9APZN20a0MaT7G2nyl0nCdp9RVb22kivrYHnNtYTkKaCgg6olF52e-cd-JbsrmnBS2qUVxV0ujn4elvpWpcf53m-yoFUrUiZUoHZ9VtFDuYCcYkQZ5PbA075AuLlJ0bOIRbf-xRiZIHwuRCcBYKTGawtQUkhg-w625AcWl1CFXKFKpAXawi69a0iUKGUJ2uCXlvqpQenFKyeinv4_bnL6LSWnVNXX_Miul4_vOSPU3LlZiDdS9pvfuzJ__rNX_pmqOrkHYS5hTk</recordid><startdate>20100601</startdate><enddate>20100601</enddate><creator>Beeren, Sophie R</creator><creator>Dabb, Serin L</creator><creator>Edwards, Gavin</creator><creator>Smith, Matthew K</creator><creator>Willis, Anthony C</creator><creator>Messerle, Barbara A</creator><scope/></search><sort><creationdate>20100601</creationdate><title>Improving intramolecular hydroamination Rh(i) and Ir(i) catalysts through targeted ligand modificationCCDC reference numbers 291181 (6), 291475 (8), 291177 (9), 291474 (10), 729970 (11). For crystallographic data in CIF or other electronic format see DOI: 10.1039/b9nj00759h</title><author>Beeren, Sophie R ; Dabb, Serin L ; Edwards, Gavin ; Smith, Matthew K ; Willis, Anthony C ; Messerle, Barbara A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_b9nj00759h3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beeren, Sophie R</creatorcontrib><creatorcontrib>Dabb, Serin L</creatorcontrib><creatorcontrib>Edwards, Gavin</creatorcontrib><creatorcontrib>Smith, Matthew K</creatorcontrib><creatorcontrib>Willis, Anthony C</creatorcontrib><creatorcontrib>Messerle, Barbara A</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beeren, Sophie R</au><au>Dabb, Serin L</au><au>Edwards, Gavin</au><au>Smith, Matthew K</au><au>Willis, Anthony C</au><au>Messerle, Barbara A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improving intramolecular hydroamination Rh(i) and Ir(i) catalysts through targeted ligand modificationCCDC reference numbers 291181 (6), 291475 (8), 291177 (9), 291474 (10), 729970 (11). For crystallographic data in CIF or other electronic format see DOI: 10.1039/b9nj00759h</atitle><date>2010-06-01</date><risdate>2010</risdate><volume>34</volume><issue>6</issue><spage>12</spage><epage>128</epage><pages>12-128</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>A series of complexes containing the phosphino-pyrazolyl ligand 1-(2-(diphenylphosphino)phenyl)pyrazole (PyPhP) and 1-(2-(diphenylphosphino)ethyl)pyrazole (PyP) were synthesized: [Ir(PyPhP)(COD)]BPh
4
, [Ir(PyPhP)(CO)
2
]BPh
4
, Rh(PyPhP)(CO)Cl and Ir(PyPhP)(CO)Cl. The complexes Rh(PyP)(CO)OSO
2
CF
3
and Rh(PyPhP)(CO)OSO
2
CF
3
were also synthesized, using the parent complexes Rh(PyP)(CO)Cl and Rh(PyPhP)(CO)Cl. The solid-state structures of the new complexes were determined by X-ray diffraction analysis. The cationic Ir(
i
) complex [Ir(PyPhP)(COD)]BPh
4
was found to be a highly efficient catalyst for the intramolecular hydroamination of 4-pentyn-1-amine, achieving a turnover rate of 1500 h
−1
, with >98% conversion in 6 minutes. The efficiency of the catalyzed hydroamination of 4-pentyn-1-amine using the neutral Ir(
i
) and Rh(
i
) complexes as catalysts was significantly improved by generating active catalysts
in situ
through abstraction of a chloride ligand by reaction with AgOSO
2
CF
3
, TMSOSO
2
CF
3
or NaBPh
4
. The catalytic efficiency of the catalysts generated from Ir(PyP)(CO)Cl and a sodium salt were found to be inversely proportional to the coordinating strength of the counter-ion of the sodium salt. Rh(PyP)(CO)OSO
2
CF
3
is a more efficient catalyst for the cyclization of 4-pentyn-1-amine than the complex generated
in situ
from AgOSO
2
CF
3
and chloride complex Rh(PyP)(CO)Cl indicating that the higher lability of the triflate co-ligand of Rh(PyP)(CO)OSO
2
CF
3
, compared to the chloride co-ligand of Rh(PyP)(CO)Cl, enhances the catalytic activity of the Rh(
i
) complexes.
Catalysed intramolecular hydroamination of 4-pentyn-1-amine was achieved with a turnover rate of 1500 h
−1
( >98% conversion in 6 minutes). Activation of catalysts
in situ
through chloride abstraction was also investigated.</abstract><doi>10.1039/b9nj00759h</doi><tpages>9</tpages></addata></record> |
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| language | eng |
| recordid | cdi_rsc_primary_b9nj00759h |
| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| title | Improving intramolecular hydroamination Rh(i) and Ir(i) catalysts through targeted ligand modificationCCDC reference numbers 291181 (6), 291475 (8), 291177 (9), 291474 (10), 729970 (11). For crystallographic data in CIF or other electronic format see DOI: 10.1039/b9nj00759h |
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