scholarly journals Local plasmon resonances of metal-in-metal core-shells

2014 ◽  
Vol 22 (3) ◽  
pp. 3186 ◽  
Author(s):  
Matthew Arnold ◽  
Martin Blaber ◽  
Mike Ford
2015 ◽  
Vol 107 (14) ◽  
pp. 141908 ◽  
Author(s):  
Ping Gu ◽  
Mingjie Wan ◽  
Qi Shen ◽  
Xiaodan He ◽  
Zhuo Chen ◽  
...  

Nanoscale ◽  
2016 ◽  
Vol 8 (19) ◽  
pp. 10358-10363 ◽  
Author(s):  
Ping Gu ◽  
Mingjie Wan ◽  
Wenyang Wu ◽  
Zhuo Chen ◽  
Zhenlin Wang

2021 ◽  
Vol 27 (S1) ◽  
pp. 2766-2768
Author(s):  
Kevin Roccapriore ◽  
Maxim Ziatdinov ◽  
Shin Hum Cho ◽  
Delia Milliron ◽  
Jordan Hachtel ◽  
...  

2018 ◽  
Vol 14 (1) ◽  
pp. 1
Author(s):  
Prof. Dr. Jamal Aziz Mehdi

The biological objectives of root canal treatment have not changed over the recentdecades, but the methods to attain these goals have been greatly modified. Theintroduction of NiTi rotary files represents a major leap in the development ofendodontic instruments, with a wide variety of sophisticated instruments presentlyavailable (1, 2).Whatever their modification or improvement, all of these instruments have onething in common: they consist of a metal core with some type of rotating blade thatmachines the canal with a circular motion using flutes to carry the dentin chips anddebris coronally. Consequently, all rotary NiTi files will machine the root canal to acylindrical bore with a circular cross-section if the clinician applies them in a strictboring manner


PIERS Online ◽  
2006 ◽  
Vol 2 (5) ◽  
pp. 450-454
Author(s):  
Norbert Riefler ◽  
Thomas Wriedt
Keyword(s):  

2001 ◽  
Vol 66 (7) ◽  
pp. 1062-1077 ◽  
Author(s):  
Maarten J. Bakker ◽  
Tapani A. Pakkanen ◽  
František Hartl

Electrochemical properties of tetrahedral clusters [H2Ru2Rh2(CO)12], [HRuRh3(CO)12] and [Rh4(CO)12] were investigated in order to evaluate the influence of metal core composition in the series [H4-xRu4-xRhx(CO)12] (x = 0-4). The cluster [H3Ru3Rh(CO)12] was not available in sufficient quantities. As reported for [H4Ru4(CO)12], electrochemical reduction of the hydride-containing clusters [H2Ru2Rh2(CO)12] and [HRuRh3(CO)12] also results in (stepwise) loss of hydrogen, producing the anions [HRu2Rh2(CO)12]-, [Ru2Rh2(CO)12]2- and [RuRh3(CO)12]-. These anions can also be prepared from the neutral parent clusters via chemical routes. Electrochemical reduction of [Rh4(CO)12] does not result in the formation of any stable tetranuclear anion. Instead, [Rh5(CO)15]- and [Rh6(CO)15]2- are the major reduction products detected in the course of IR spectroelectrochemical experiments. Most likely, these cluster species are formed from the secondary CO-loss product [Rh4(CO)11]2- by fast redox condensation reactions. Their reoxidation regenerates parent [Rh4(CO)12], together with some [Rh6(CO)16]. Unlike [H4Ru4(CO)12] that undergoes photochemical CO-dissociation, [H2Ru2Rh2(CO)12] and [Rh4(CO)12] are completely photostable in neat hexane and dichloromethane as well as in the presence of oct-1-ene.


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