PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
27110904-1	2016	Electrocatalytic CO2 reduction to CO was achieved with a novel Mn complex, fac-[MnBr(4,4"-bis(phosphonic acid)-2,2"-bipyridine)(CO)3 ] (MnP), immobilized on a mesoporous TiO2 electrode.	Carbon Monoxide	17-19	FA complementation group C	Homo sapiens	75-78	
27722517-1	2016	fac-[Re(CO)3(dppz)] complexes of amido ligands generated in situ under basic conditions display an intense (epsilon = 16460 L mol-1 cm-1) absorption band between 500-700 nm which are assigned to an n(amido,RNH-)   pi* (dppz) inter-ligand charge transfer band offering an extraordinarily low energy charge separating absorption with potential for imaging and energy application.	Carbon Monoxide	8-10	FA complementation group C	Homo sapiens	0-3	
24053131-1	2013	A complete mechanism for the proton-dependent electrocatalytic reduction of CO2 to CO by fac-Re(bpy)(CO)3Cl that is consistent with experimental observations has been developed using first principles quantum chemistry.	Carbon Monoxide	76-78	FA complementation group C	Homo sapiens	89-92	
26068141-5	2015	We report here NMR, molecular (X-ray) structure, and solution data on fac-[Re(I)(CO)3(NTA)](2-) with a -CH2CO2(-) dangling monoanionic chain and on two fac-[Re(I)(CO)3(L)](-) analogues with either a -CH2CONH2 or a -CH2CH2OH dangling neutral chain.	Carbon Monoxide	81-83	FA complementation group C	Homo sapiens	70-73	
15702193-0	2005	The chemistry of the fac-[Re(CO)2(NO)]2+ fragment in aqueous solution.	Carbon Monoxide	29-32	FA complementation group C	Homo sapiens	21-24	
16472004-2	2006	Solution-phase continuous and laser flash photolysis of the tetraphenylarsonium salt of the fac-[CH3Ir(CO)2I3]- anion (1a) under excess carbon monoxide resulted in migratory insertion to give the acyl complex ion mer,trans-[Ir(C(O)CH3)(CO)2I3]- (2a).	Carbon Monoxide	136-151	FA complementation group C	Homo sapiens	92-95	
32585094-3	2020	We report herein that complex fac-[MnI(bis-MesNHC)(CO)3Br] [1; bis-MesNHC = 3,3-bis(2,4,6-trimethylphenyl)-(1,1"-diimidazolin-2,2"-diylidene)methane] could catalyze the electrochemical reduction of CO2 to CO with high activity (TOFmax = 3180 +- 6 s-1) at a less negative potential.	Carbon Monoxide	51-53	FA complementation group C	Homo sapiens	30-33	
29740881-0	2018	Electrospray ionization study of tricarbonyl fac-[Re(CO)3 (PO)(X)]-type complexes: influence of ancillary co-ligands in the release of carbon monoxide.	Carbon Monoxide	135-150	FA complementation group C	Homo sapiens	45-48	
29740881-1	2018	RATIONALE: fac-[Re(CO)3 (PO)(X)]-type complexes (PO = chelated bidentate tertiary phosphine (1-), X = various neutral, mono-dentate ligands) represent a class of compounds that meets the synthetic criteria for the preparation of potential carbon monoxide (CO) release molecules (CORMs) for medicinal application.	Carbon Monoxide	239-254	FA complementation group C	Homo sapiens	11-14	
29740881-1	2018	RATIONALE: fac-[Re(CO)3 (PO)(X)]-type complexes (PO = chelated bidentate tertiary phosphine (1-), X = various neutral, mono-dentate ligands) represent a class of compounds that meets the synthetic criteria for the preparation of potential carbon monoxide (CO) release molecules (CORMs) for medicinal application.	Carbon Monoxide	19-21	FA complementation group C	Homo sapiens	11-14	
29481726-1	2018	We report here the first purely organometallic fac-[MnI (CO)3 (bis-Me NHC)Br] complex with unprecedented activity for the selective electrocatalytic reduction of CO2 to CO, exceeding 100 turnovers with excellent faradaic yields (etaCO  95 %) in anhydrous CH3 CN.	Carbon Monoxide	57-59	FA complementation group C	Homo sapiens	47-50