361375-52-2

Upstream product

• 64-19-7 acetic acid 
• 603-35-0 triphenylphosphine 

Downstream Products

• 361370-26-5 Rh₂(C₄H₄NO₂)2(C₆H₄P(C₆H₅)2)2 
• 361370-26-5 Rh₂(C₄H₄NO₂)2(C₆H₄P(C₆H₅)2)2 

Relevant academic research and scientific papers

Chiral organometallic triangles with Rh-Rh bonds. 2. Compounds prepared from enantiopure cis-Rh2(C6H4PPh 2)2(OAc)2(HOAc)2 and their catalytic potentials

Enantiomers of the orthometalated dirhodium compound cis-Rh 2(C6H4PPh2)2(OAc) 2(HOAc)2 (R-1 and S-1) were prepared from carboxylate exchange reactions of the resolved diasteroiso

Detection of Neutral CO Lost During Ionic Dissociation Using Atmospheric Pressure Thermal Dissociation Mass Spectrometry (APTD-MS)

Elucidation of ion dissociation patterns is particularly important to structural analysis by mass spectrometry (MS). However, typically, only the charged fragments from an ion dissociation event are detected in tandem MS experiments; neutrals are not identified. In recent years, we have developed an atmospheric pressure thermal dissociation (APTD) technique that can be applied to dissociate ions at atmosphere pressure and thus provide one way to characterize neutral fragments. In this paper, we focus on the detection of neutral CO resulting from amino acid and peptide ion dissociation. In the first set of experiments, several protonated amino acids (e.g., + 1 ion of phenylalanine) were found to undergo loss of a neutral (s) of total mass 46?Da, a process leading to iminium ion formation. We successfully detected the neutral species CO by using a CO sensor, UV-Vis and MS analysis following selective CO trapping with a rhodium complex. The capture of CO from dissociation of protonated amino acids supports the assignment of the loss of 46?Da to neutral losses of CO and H2O, rather than loss of formaldehyde or dihydroxycarbene, other possible fragmentation pathways that have been subject of debate for a long time. In a second experiment, we used the APTD method in combination with the CO detection technique, to demonstrate the formation of CO in the conversion of b ions to a ions during peptide ion dissociations. These results showed the potential of APTD in the elucidation of ion dissociation mechanisms, using simple home-built apparatus. [Figure not available: see fulltext.].