Literature DB >> 11884750

Singlet diradicals: from transition states to crystalline compounds.

David Scheschkewitz1, Hideki Amii, Heinz Gornitzka, Wolfgang W Schoeller, Didier Bourissou, Guy Bertrand.   

Abstract

Singlet diradicals are usually not energy minima. As observed by femtosecond spectroscopy, they readily couple to form final sigma bonds. Substituent effects allow lifetimes to increase into the microsecond range. Taking advantage of the properties of hetero-elements, a diradical has been prepared that is indefinitely stable at room temperature. The availability of diradicals that can be handled under standard laboratory conditions will lead to further insight into their chemical and physical properties, raising the likelihood of practical applications, especially in the field of molecular materials such as electrical conductors and ferromagnets.

Year:  2002        PMID: 11884750     DOI: 10.1126/science.1068167

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  15 in total

1.  Stable singlet carbenes as mimics for transition metal centers.

Authors:  David Martin; Michele Soleilhavoup; Guy Bertrand
Journal:  Chem Sci       Date:  2011-01-01       Impact factor: 9.825

Review 2.  Stable cyclic carbenes and related species beyond diaminocarbenes.

Authors:  Mohand Melaimi; Michèle Soleilhavoup; Guy Bertrand
Journal:  Angew Chem Int Ed Engl       Date:  2010-11-15       Impact factor: 15.336

3.  Carbene-Stabilized Main Group Radicals and Radical Ions.

Authors:  Caleb D Martin; Michele Soleilhavoup; Guy Bertrand
Journal:  Chem Sci       Date:  2013-08-01       Impact factor: 9.825

4.  Main-group elements as transition metals.

Authors:  Philip P Power
Journal:  Nature       Date:  2010-01-14       Impact factor: 49.962

5.  Thermally controlling the singlet-triplet energy gap of a diradical in the solid state.

Authors:  Yuanting Su; Xingyong Wang; Lei Wang; Zaichao Zhang; Xinping Wang; You Song; Philip P Power
Journal:  Chem Sci       Date:  2016-06-28       Impact factor: 9.825

6.  Substituent effect on the energy barrier for σ-bond formation from π-single-bonded species, singlet 2,2-dialkoxycyclopentane-1,3-diyls.

Authors:  Jianhuai Ye; Yoshihisa Fujiwara; Manabu Abe
Journal:  Beilstein J Org Chem       Date:  2013-05-14       Impact factor: 2.883

7.  Recent developments in and perspectives on three-coordinate boron materials: a bright future.

Authors:  Lei Ji; Stefanie Griesbeck; Todd B Marder
Journal:  Chem Sci       Date:  2016-11-09       Impact factor: 9.825

8.  Zwitterionic and biradicaloid heteroatomic cyclopentane derivatives containing different group 15 elements.

Authors:  Alexander Hinz; Axel Schulz; Alexander Villinger
Journal:  Chem Sci       Date:  2015-10-27       Impact factor: 9.825

9.  Equilibrium Formation of Stable All-Silicon Versions of 1,3-Cyclobutanediyl.

Authors:  Cem B Yildiz; Kinga I Leszczyńska; Sandra González-Gallardo; Michael Zimmer; Akin Azizoglu; Till Biskup; Christopher W M Kay; Volker Huch; Henry S Rzepa; David Scheschkewitz
Journal:  Angew Chem Int Ed Engl       Date:  2020-06-15       Impact factor: 16.823

10.  Silicon-silicon π single bond.

Authors:  Soichiro Kyushin; Yoshikuni Kurosaki; Kyohei Otsuka; Haruna Imai; Shintaro Ishida; Toru Kyomen; Minoru Hanaya; Hideyuki Matsumoto
Journal:  Nat Commun       Date:  2020-08-11       Impact factor: 17.694

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