Weak Intramolecular Exchange Interaction between Two Carbenic Units in a Novel Organic High-Spin Ion. ESR Studies on a Monoanion of Biphenyl-3,3'-diylbis(phenylmethylene)

1995 ◽  
Vol 117 (45) ◽  
pp. 11292-11298 ◽  
Author(s):  
Toshihiro Nakamura ◽  
Takamasa Momose ◽  
Tadamasa Shida ◽  
Takamasa Kinoshita ◽  
Takeji Takui ◽  
...  
2007 ◽  
Author(s):  
Y. Shvachko ◽  
D. Starichenko ◽  
A. Korolev ◽  
V. Ustinov ◽  
D. Boukhvalov ◽  
...  

2004 ◽  
pp. 2050-2051 ◽  
Author(s):  
Christophe Stroh ◽  
Marcel Mayor ◽  
Carsten von Hänisch ◽  
Philippe Turek

2011 ◽  
Vol 21 (2) ◽  
pp. 137
Author(s):  
Nguyen Anh Tuan ◽  
Nguyen Van Thanh ◽  
Tran Thi Thuy Nu ◽  
Nguyen Huy Sinh ◽  
Vu Van Khai ◽  
...  

The geometric and electronic structures of [Mn44+Mn3+3(µ3-L2 -)3(µ3-X -(OAc) - 3(dbm) -3] (L = O, X = F, dbmH = dibenzoyl-methane) molecule has been studied by first-principles calculations. It was shown in our previous paper that the ferrimagnetic structure of Mn$^{4 + }$Mn$^{3 + }_{3}$ molecules is determined by the $\pi $ type hybridization between the $d_{z^2}$ orbitals at the three high-spin Mn$^{3 + }$ ions and the $t_{2g}$ orbitals at the Mn$^{4 + }$ ion by the $p$ orbitals at the $\mu _{3}$-L$^{2 - }$ ions. To design new Mn$^{4 + }$Mn$^{3 + }_{3}$ molecules having much more stable ferrimagnetic state, one approach is suggested. That is controlling the Mn$^{4 + }$-($\mu _{3}$-L$^{2 - })$-Mn$^{3 + }$ exchange pathways by rational variation in $\mu _{3}$-L ligands to strengthen the hybridization between Mn ions. By this ligand variation, $J_{AB}$ can be enhanced by a factor of 3. Our results should facilitate the rational synthesis of new single-molecule magnets.


2020 ◽  
Vol 26 (14) ◽  
pp. 3166-3172 ◽  
Author(s):  
Atsuki Nagata ◽  
Shinsuke Hiraoka ◽  
Shuichi Suzuki ◽  
Masatoshi Kozaki ◽  
Daisuke Shiomi ◽  
...  

1992 ◽  
Vol 52 (1) ◽  
pp. 71-85 ◽  
Author(s):  
Nikolay Tyutyulkov ◽  
Stoyan Karabunarliev ◽  
Klaus Müllen ◽  
Martin Baumgarten

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