scholarly journals Organometallic Phosphinimines as Building Blocks for Potential New Radiopharmaceuticals. Synthesis, Structure and Reactivity of Ph3P=NH2+ReO4-

1993 ◽  
Vol 48 (10) ◽  
pp. 1381-1385 ◽  
Author(s):  
Kattesh V. Katti ◽  
Prahlad R. Singh ◽  
Charles L. Barnes ◽  
Kavita K. Katti ◽  
Karel Kopicka ◽  
...  

Reactions of the organometallic phosphinimine Ph3P=N-SiMe3 (1), with aqueous ReO4- and 188ReO4- yield the ion pairs Ph3P=NH2+MO4- (M=Re (2); 188Re (4)). The ion pairs undergo dehydration upon heating to produce the neutral Re(VII) species: Ph3P=N-MO3 (M=Re (3); 188Re (5)). The solid state structure of Ph3P=NH2+ReO4- (2) shows the presence of hydrogen bonding between the iminato hydrogen and the rhenium oxo center. The relevance of such reactions for the design of new radiopharmaceuticals is discussed

2015 ◽  
Vol 71 (10) ◽  
pp. o697-o698 ◽  
Author(s):  
Francesca A. Vaccaro ◽  
Lynn V. Koplitz ◽  
Joel T. Mague

The asymmetric unit of the title salt, C7H7N2+·BF4−, comprises two independent but nearly identical formula units. The solid-state structure comprises corrugated layers of cations and anions, formed by C—H...F hydrogen bonding, that are approximately parallel to (010). Further C—H...F hydrogen bonding consolidates the three-dimensional architecture. The sample was refined as a two-component non-merohedral twin.


RSC Advances ◽  
2017 ◽  
Vol 7 (11) ◽  
pp. 6236-6241 ◽  
Author(s):  
Tomoaki Kanetou ◽  
Ryo Tsunashima ◽  
Norihisa Hoshino ◽  
Tomoyuki Akutagawa

Our results clarified uniqueness in hydrogen bonding TTFPy dimer in which proton in hydrogen bond was thermally fluctuated. In addition, the fluctuation was coupled with π-electronic systems of TTF moiety where electric dipole moment was amplified.


2003 ◽  
Vol 666 (1-2) ◽  
pp. 49-53 ◽  
Author(s):  
Donald J Darensbourg ◽  
Andrea L Phelps ◽  
M.Jason Adams ◽  
Jason C Yarbrough

2019 ◽  
Vol 55 (26) ◽  
pp. 3761-3764 ◽  
Author(s):  
Timothy G. Carroll ◽  
Camden Hunt ◽  
Rachel Garwick ◽  
Guang Wu ◽  
Roman Dobrovetsky ◽  
...  

A C3v-symmetric triarylphosphine oxide locked into conformation by H-bonding and displaying an extended MOF-like solid-state structure is reported.


2017 ◽  
Vol 46 (5) ◽  
pp. 1645-1659 ◽  
Author(s):  
Janek Tomaschautzky ◽  
Beate Neumann ◽  
Hans-Georg Stammler ◽  
Andreas Mix ◽  
Norbert W. Mitzel

Triphenylsilanes are versatile propeller-shaped building blocks and have been used for the syntheses of several novel poly-Lewis-acids. The first solid-state structure of a bisma-silatriptycene as well as investigations in host–guest chemistry of a triple alane with a threefold amine are reported.


2004 ◽  
Vol 60 (4) ◽  
pp. m441-m443 ◽  
Author(s):  
Christopher Bresner ◽  
Simon Aldridge ◽  
Ian A. Fallis ◽  
Li-Ling Ooi

2015 ◽  
Vol 71 (11) ◽  
pp. o852-o853
Author(s):  
Vu D. Nguyen ◽  
Cameron A. McCormick ◽  
Joel T. Mague ◽  
Lynn V. Koplitz

The asymmetric unit of the title salt, C7H7N2+·ClO4−, comprises two independent formula units. The solid-state structure comprises corrugated layers of cations and of anions, approximately parallel to (010). The supramolecular layers are stabilized and connected by C—H...O hydrogen bonding to consolidate a three-dimensional architecture. A close pyridinium–perchlorate N...O contact [2.867 (5) Å] is noted. The crystal was refined as an inversion twin.


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