Matches in SemOpenAlex for { <https://semopenalex.org/work/W2020091910> ?p ?o ?g. }
- W2020091910 endingPage "271" @default.
- W2020091910 startingPage "247" @default.
- W2020091910 abstract "The cyclic six-membered thionylphosphazenes, (NPCl2)2[NS(O)X] X=Cl (1), Ph (2) and 4-ClC6H4 (3) as well as the monospirocyclic derivatives (NPCl2)NP[N(Me)CH2]2[NS(O)Ph] (4) and (NPCl2)NP[N(Me)CH2]2[NS(O)4-ClC6H4] (5) were synthesized. Reactions of these compounds were carried out with dilithiated ferrocene-derived hydroxymethyl phosphine sulfides, FcCH2P(S)(CH2OH)2 (6) and FcCH(CH3)P(S)(CH2OH)2 (7) under different conditions. Reactions of 1 with 6 and 7 did not yield any desired products. In contrast, 1:1 reactions of 2 with 6 and 7 readily yielded air stable monospirocyclic compounds FcCH2P(S)(CH2O)2PN(NPCl2)[NS(O)Ph] (8) and FcCH(CH3)P(S)(CH2O)2PN(NPCl2)[NS(O)Ph] (9), respectively. Controlled reactions of 4 and 5 with 6 were performed in which dispirocyclic compounds FcCH2P(S)(CH2O)2PN2P[N(Me)CH2]2[NS(O)Ph] (10) and FcCH2P(S)(CH2O)2PN2P[N(Me)CH2]2[NS(O)4-ClC6H4] (11) were isolated. The product obtained in the 1:1 reaction of HOCH2(CF2)2CH2OH with (NPCl2)2[NS(O)4-ClC6H4] (3) when reacted with 6 resulted in the dispirocyclic compound FcCH2P(S)[(CH2O)2PN2P (OCH2CF2)2][NS(O)4-ClC6H4] (12). Compound 12 was found to exist as isomers. To confirm the formation of isomers, {[CH2N(Me)]2PN2P(OCH2CF2)2}[NS(O)Ph] (13) was synthesized by the reaction of 4 with HOCH2(CF2)2CH2OH which was also found to exist as isomers. Attempts to synthesize intermolecular bridged compounds of 2 with 6 and 7 resulted in compounds 8 and 9 exclusively. The crystal structures of compounds 8 and 10 were determined." @default.
- W2020091910 created "2016-06-24" @default.
- W2020091910 creator A5090493954 @default.
- W2020091910 date "1992-01-01" @default.
- W2020091910 modified "2023-10-16" @default.
- W2020091910 title "Selected chemistry of cyclophosphazenes and cyclothiaphosphazenes" @default.
- W2020091910 cites W1489787941 @default.
- W2020091910 cites W1513254937 @default.
- W2020091910 cites W1577976968 @default.
- W2020091910 cites W1580011122 @default.
- W2020091910 cites W1624376690 @default.
- W2020091910 cites W1676608665 @default.
- W2020091910 cites W1938190284 @default.
- W2020091910 cites W1966725510 @default.
- W2020091910 cites W1966893745 @default.
- W2020091910 cites W1970423440 @default.
- W2020091910 cites W1973657294 @default.
- W2020091910 cites W1976191136 @default.
- W2020091910 cites W1977214000 @default.
- W2020091910 cites W1977724127 @default.
- W2020091910 cites W1977874766 @default.
- W2020091910 cites W1978548037 @default.
- W2020091910 cites W1978864324 @default.
- W2020091910 cites W1982009176 @default.
- W2020091910 cites W1985566812 @default.
- W2020091910 cites W1986167346 @default.
- W2020091910 cites W1991524118 @default.
- W2020091910 cites W1996120625 @default.
- W2020091910 cites W1998727828 @default.
- W2020091910 cites W1999140835 @default.
- W2020091910 cites W2001471784 @default.
- W2020091910 cites W2004879686 @default.
- W2020091910 cites W2017201066 @default.
- W2020091910 cites W2022086142 @default.
- W2020091910 cites W2027846485 @default.
- W2020091910 cites W2028917996 @default.
- W2020091910 cites W2030104044 @default.
- W2020091910 cites W2030392804 @default.
- W2020091910 cites W2031791290 @default.
- W2020091910 cites W2032147765 @default.
- W2020091910 cites W2033303797 @default.
- W2020091910 cites W2037409787 @default.
- W2020091910 cites W2039098534 @default.
- W2020091910 cites W2039938192 @default.
- W2020091910 cites W2040054853 @default.
- W2020091910 cites W2040491926 @default.
- W2020091910 cites W2041505958 @default.
- W2020091910 cites W2041622007 @default.
- W2020091910 cites W2041860978 @default.
- W2020091910 cites W2042906944 @default.
- W2020091910 cites W2047012837 @default.
- W2020091910 cites W2047630464 @default.
- W2020091910 cites W2055287742 @default.
- W2020091910 cites W2056020082 @default.
- W2020091910 cites W2057329060 @default.
- W2020091910 cites W2059701028 @default.
- W2020091910 cites W2060553534 @default.
- W2020091910 cites W2060710287 @default.
- W2020091910 cites W2063508338 @default.
- W2020091910 cites W2065661925 @default.
- W2020091910 cites W2066432398 @default.
- W2020091910 cites W2066654495 @default.
- W2020091910 cites W2069734849 @default.
- W2020091910 cites W2072883484 @default.
- W2020091910 cites W2073543952 @default.
- W2020091910 cites W2073692318 @default.
- W2020091910 cites W2076489400 @default.
- W2020091910 cites W2086499505 @default.
- W2020091910 cites W2088556222 @default.
- W2020091910 cites W2088976690 @default.
- W2020091910 cites W2092522733 @default.
- W2020091910 cites W2100201484 @default.
- W2020091910 cites W2102982465 @default.
- W2020091910 cites W2104698841 @default.
- W2020091910 cites W2106967960 @default.
- W2020091910 cites W2109148664 @default.
- W2020091910 cites W2109207609 @default.
- W2020091910 cites W2121720810 @default.
- W2020091910 cites W2124109342 @default.
- W2020091910 cites W2131700440 @default.
- W2020091910 cites W2133547070 @default.
- W2020091910 cites W2134180524 @default.
- W2020091910 cites W2135177771 @default.
- W2020091910 cites W2142419928 @default.
- W2020091910 cites W2153107925 @default.
- W2020091910 cites W2154404718 @default.
- W2020091910 cites W2155329934 @default.
- W2020091910 cites W2159980887 @default.
- W2020091910 cites W2161137852 @default.
- W2020091910 cites W2272680903 @default.
- W2020091910 cites W2313557917 @default.
- W2020091910 cites W2322468335 @default.
- W2020091910 cites W2323759014 @default.
- W2020091910 cites W2324303802 @default.
- W2020091910 cites W2326545180 @default.
- W2020091910 cites W2328605812 @default.
- W2020091910 cites W234676629 @default.
- W2020091910 cites W2396383492 @default.