New Adamantane-like Silicophosphate Cage and Its Reactivity
toward Tris(pentafluorophenyl)borane

J 2017

New Adamantane-like Silicophosphate Cage and Its Reactivity toward Tris(pentafluorophenyl)borane

STÝSKALÍK, Aleš, Michal BABIAK, Petr MACHÁČ, Bohuslava RELICHOVÁ, Jiří PINKAS et. al.

Základní údaje

Originální název

New Adamantane-like Silicophosphate Cage and Its Reactivity toward Tris(pentafluorophenyl)borane

Autoři

STÝSKALÍK, Aleš (203 Česká republika, domácí), Michal BABIAK (703 Slovensko, domácí), Petr MACHÁČ (203 Česká republika, domácí), Bohuslava RELICHOVÁ (203 Česká republika, domácí) a Jiří PINKAS (203 Česká republika, garant, domácí)

Vydání

Inorganic Chemistry, WASHINGTON, American Chemical Society, 2017, 0020-1669

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10402 Inorganic and nuclear chemistry

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 4.700

Kód RIV

RIV/00216224:14310/17:00098061

Organizační jednotka

Přírodovědecká fakulta

DOI

http://dx.doi.org/10.1021/acs.inorgchem.7b01572

UT WoS

000410005600064

Klíčová slova anglicky

silicophosphate; boranes; enantiomers; adamantane; conglomerate of homochiral crystals

Štítky

CF NMR, CF SAXS, NZ, rivok

Příznaky

Mezinárodní význam, Recenzováno

Změněno: 9. 4. 2018 16:14, Ing. Nicole Zrilić

Anotace

V originále

The condensation reaction between Ph2Si(OC-(O)CH3)(2) and OP(OSiMe3)(3) leads to elimination of CH3C(O)OSiMe3 and the formation of the new silicophosphate cage molecule Ph12Si6P4O16 (1) with an adamantane-like core possessing four terminal P=O moieties and six OSiPh2O bridging groups. Compound 1 was further reacted with the Lewis acid B(C6F5)3. We observed adduct formation by coordination through the P=O -> B bonds and isolated and structurally characterized two new molecules. In the first of them, the adamantane-like cage is preserved and three phosphoryl oxygen atoms coordinate to boranes, forming Ph12Si6O16P4 center dot 3B(C6F5)(3) (2); the remaining P=O group is inverted toward the cage center pointing along a C-3 molecular axis. The molecule is chiral, and the compound 2 crystallizes as a conglomerate of homochiral crystals. Enantiomers 2M and 2P were both structurally characterized. The second adduct resulted from an unexpected reorganization of the SiOP linkages in the adamantane cage during the reaction of 1 with 4 equiv of B(C6F5)(3). The bis-adduct Ph6Si3O8P2 center dot 2B(C6F5)(3) (3) was formed with an inorganic core representing half of the parent molecule 1.

Návaznosti

LM2015043, projekt VaV

Název: Česká infrastruktura pro integrativní strukturní biologii (Akronym: CIISB)

Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Czech Infrastructure for Integrative Structural Biology

LQ1601, projekt VaV

Název: CEITEC 2020 (Akronym: CEITEC2020)

Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, CEITEC 2020

Citovat

STÝSKALÍK, Aleš, Michal BABIAK, Petr MACHÁČ, Bohuslava RELICHOVÁ a Jiří PINKAS. New Adamantane-like Silicophosphate Cage and Its Reactivity toward Tris(pentafluorophenyl)borane. Inorganic Chemistry. WASHINGTON: American Chemical Society, 2017, roč. 56, č. 17, s. 10699-10705. ISSN 0020-1669. Dostupné z: https://dx.doi.org/10.1021/acs.inorgchem.7b01572.

@article{1393656,
   author = {Stýskalík, Aleš and Babiak, Michal and Macháč, Petr and Relichová, Bohuslava and Pinkas, Jiří},
   article_location = {WASHINGTON},
   article_number = {17},
   doi = {http://dx.doi.org/10.1021/acs.inorgchem.7b01572},
   keywords = {silicophosphate; boranes; enantiomers; adamantane; conglomerate of homochiral crystals},
   language = {eng},
   issn = {0020-1669},
   journal = {Inorganic Chemistry},
   title = {New Adamantane-like Silicophosphate Cage and Its Reactivity toward Tris(pentafluorophenyl)borane},
   volume = {56},
   year = {2017}
}

TY  - JOUR
ID  - 1393656
AU  - Stýskalík, Aleš - Babiak, Michal - Macháč, Petr - Relichová, Bohuslava - Pinkas, Jiří
PY  - 2017
TI  - New Adamantane-like Silicophosphate Cage and Its Reactivity toward Tris(pentafluorophenyl)borane
JF  - Inorganic Chemistry
VL  - 56
IS  - 17
SP  - 10699-10705
EP  - 10699-10705
PB  - American Chemical Society
SN  - 00201669
KW  - silicophosphate
KW  - boranes
KW  - enantiomers
KW  - adamantane
KW  - conglomerate of homochiral crystals
N2  - The condensation reaction between Ph2Si(OC-(O)CH3)(2) and OP(OSiMe3)(3) leads to elimination of CH3C(O)OSiMe3 and the formation of the new silicophosphate cage molecule Ph12Si6P4O16 (1) with an adamantane-like core possessing four terminal P=O moieties and six OSiPh2O bridging groups. Compound 1 was further reacted with the Lewis acid B(C6F5)3. We observed adduct formation by coordination through the P=O -> B bonds and isolated and structurally characterized two new molecules. In the first of them, the adamantane-like cage is preserved and three phosphoryl oxygen atoms coordinate to boranes, forming Ph12Si6O16P4 center dot 3B(C6F5)(3) (2); the remaining P=O group is inverted toward the cage center pointing along a C-3 molecular axis. The molecule is chiral, and the compound 2 crystallizes as a conglomerate of homochiral crystals. Enantiomers 2M and 2P were both structurally characterized. The second adduct resulted from an unexpected reorganization of the SiOP linkages in the adamantane cage during the reaction of 1 with 4 equiv of B(C6F5)(3). The bis-adduct Ph6Si3O8P2 center dot 2B(C6F5)(3) (3) was formed with an inorganic core representing half of the parent molecule 1.
ER  -

STÝSKALÍK, Aleš, Michal BABIAK, Petr MACHÁČ, Bohuslava RELICHOVÁ a Jiří PINKAS. New Adamantane-like Silicophosphate Cage and Its Reactivity toward Tris(pentafluorophenyl)borane. \textit{Inorganic Chemistry}. WASHINGTON: American Chemical Society, 2017, roč.~56, č.~17, s.~10699-10705. ISSN~0020-1669. Dostupné z: https://dx.doi.org/10.1021/acs.inorgchem.7b01572.

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