Archive for July, 2015

July’s HOT articles

Take a look at our HOT articles for July. These are only free to acess for 4 weeks only and are available for viewing in a collection on our website.

A mononuclear Ni(II) complex: a field induced single-molecule magnet showing two slow relaxation processes
Jozef Miklovič, Dušan Valigura, Roman Boča and Ján Titiš
Dalton Trans., 2015, 44, 12484-12487
DOI: 10.1039/C5DT01213A

Graphical Abstract

  

Free to access until 6th August 2015 

 


 ZnII and HgII binding to a designed peptide that accommodates different coordination geometries
Dániel Szunyogh, Béla Gyurcsik, Flemming H. Larsen, Monika Stachura, Peter W. Thulstrup, Lars Hemmingsen and Attila Jancsó
Dalton Trans., 2015, 44, 12576-12588
DOI: 10.1039/C5DT00945F 

Graphical Abstract 

Free to access until 6th August 2015  


 

Photophysical tuning of the aggregation-induced emission of a series of para-substituted aryl bis(imino)acenaphthene zinc complexes
Daniel A. Evans, Lucia Myongwon Lee, Ignacio Vargas-Baca and Alan H. Cowley
Dalton Trans., 2015, 44, 11984-11996
DOI: 10.1039/C5DT01529D 

Graphical Abstract

Free to access until 6th August 2015


An investigation into the photochemistry of, and the electrochemically induced CO-loss from, [(CO)5MC(OMe)Me](M = Cr or W) using low-temperature matrix isolation, picosecond infrared spectroscopy, cyclic voltammetry, and time-dependent density functional theory 
Suzanne McMahon, Saeed Amirjalayer, Wybren J. Buma, Yvonne Halpin, Conor Long, A. Denise Rooney, Sander Woutersen and Mary T. Pryce
Dalton Trans., 2015, Advance Article 
DOI: 10.1039/C5DT01568E

Graphical Abstract

Free to access until 6th August 2015


Aza-macrocyclic complexes of the Group 1 cations – synthesis, structures and density functional theory study
John Dyke, William Levason, Mark E. Light, David Pugh, Gillian Reid, Hanusha Bhakhoa, Ponnadurai Ramasami and Lydia Rhyman  
Dalton Trans., 2015, Advance Article  
DOI: 10.1039/C5DT01865J  

Graphical Abstract

Free to access until 6th August 2015


As-stereogenic C2-symmetric organoarsines: synthesis and enantioselective self-assembly into a dinuclear triple-stranded helicate with copper iodide
Hiroki Adachi, Hiroaki Imoto, Seiji Watase, Kimihiro Matsukawa and Kensuke Naka 
Dalton Trans., 2015, Advance Article  
DOI: 10.1039/C5DT01490E  

Graphical Abstract

Free to access until 6th August 2015

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The Crystal Field Theory They Didn’t Teach You in Undergrad

To me the most interesting observation in the recent Dalton Transactions paper from the group of Professor Phil Power was their suggestion that secondary interactions between dicoordinate Fe(II) atoms and carbon atoms on their ligands probably have a significant effect on the magnetic moment of the complexes.

Specifically, they postulate that these interactions help to quench the orbital contribution to the magnetic moment, which is significant for other dicoordinate Fe(II) complexes studied.

But let’s take a step back.  Dicoordinate Iron(II) complexes were unknown until the 1980’s, thought to be too unstable to isolate and structurally characterize.  As the authors detail, examples were discovered gradually. All featuring large coordinating ligands bound through anionic C, N, or O donors.  Power reports a total of thirty currently known.

No one, it appears, has previously undertaken thorough magnetic studies.  Indeed, do you remember studying how crystal field theory applies to dicoordinate metal species in your introductory inorganic class?  I don’t.

The authors focus their attention on four species. Two of these feature large silylamido ligands and have solid-state N-Fe-N angles of 169o and 172o, the other have two large aryl ligands and exhibit slightly more bent geometries.  The authors support the evidence that a significant part of the measured temperature-dependent magnetic moment of these molecules arises from the orbital contribution – that is, from the motion of electrons around the iron nucleus, rather than arising only from the spin contribution, the electrons spinning about their own axes.

However, the less linear aryl iron(ll) complexes show the greater orbital contribution to the magnetic moment, which brings me back to the beginning.  This is a thorough paper; the authors also construct a spectrochemical series for the dicoordinate Fe(II) complexes and exactingly compare computed and experimental magnetic data.  But the original small structure-function observation fascinated me on my first reading.

Read the full article now:

Ligand field influence on the electronic and magnetic properties of quasi-linear two-coordinate iron(II) complexes
Nicholas F. Chilton, Hao Lei, Aimee M. Bryan, Fernande Grandjean, Gary J. Long and Philip P. Power
Dalton Trans., 2015, 44, 11202-11211
DOI: 10.1039/C5DT01589H


Ian Mallov Ian Mallov is currently a Ph.D. student in Professor Doug Stephan’s group at the University of Toronto. His research is focused on synthesizing new Lewis-acidic compounds active in Frustrated Lewis Pair chemistry. He grew up in Truro, Nova Scotia and graduated from Dalhousie University and the University of Ottawa, and worked in chemical analysis in industry for three years before returning to grad school.
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