From the Nonexistent Polar Intermetallic Pt3Pr4 via Pt2–xPr3 to Pt/Sn/Pr Ternaries
Author(s) -
Melissa L. Rhodehouse,
Thomas Bell,
Volodymyr Smetana,
AnjaVerena Mudring,
Gerd Meyer
Publication year - 2018
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.8b01121
Subject(s) - intermetallic , chemistry , crystallography , phase diagram , tin , metal , transition metal , ternary operation , crystal structure , phase (matter) , alloy , catalysis , biochemistry , organic chemistry , computer science , programming language
Although the Pt-Pr phase diagram has been explored well, recent work on rare-earth metal cluster halides with endohedral transition metal atoms has provided a new binary intermetallic that is nonexistent in the known phase diagram: The binary P 3 Pr 4 (1) crystallizes in a new structure type ( mP56, P2 1 / c, a = 12.353(2) Å, b = 7.4837(9) Å, c = 17.279(2) Å, β = 118.003(7)°, Z = 8) with six crystallographically independent Pt as well as eight Pr positions. The subsequent detailed investigation has led to another previously unreported, binary phase with the Ga 2 Gd 3 structure type, P 2- x Pr 3 (2, tI80, I4/ mcm, a = 11.931(9) Å, c = 14.45(1) Å, Z = 16), that is practically overlapping with the rhombohedral P 2 Pr 3 existing in the phase diagram. Application of different tin containing fluxes to reproduce the newly detected phases brought about two almost iso-compositional ternary compounds with Sn, P 4 Sn 6 Pr 2.91 (3), and P 4 Sn 6 Pr 3 (4), as well as P 12 Sn 24 Pr 4.84 (5). 3 is a representative of the P 4 Ge 6 Ce 3 ype ( oP52, Pnma, a = 7.2863(3) Å, b = 4.4909(2) Å, c = 35.114(2) Å), while 4 represents a new variant of the prolific T 4 E 6 R 3 family ( T = transition metal, E = main group (semi)metal, R = rare-earth metal; P 4 Sn 6 Pr 3 : oP52, Pnma, a = 27.623(1) Å, b = 4.5958(2) Å, c = 9.3499(5) Å). P 12 Sn 24 Pr 5- x (5) crystallizes as a variant of the Ni 8 Sn 16 Gd 3 ype ( cI82, Im3̅, a = 12.274(1) Å, Z = 2). Electronic structure calculations provide hints on the origin of the structural changes ( pseudo-polymorphism) for P x Pr 3 with x = 1.97 and 2.00, respectively, and reveal that heteroatomic Pt-Pr bonding strongly dominates in both binaries while the addition of the reactive metal tin leads to dominating Pt-Sn bonding interactions in the ternaries; Pt-Pt bonding interactions are strong but represent a minority in the binaries and are not present at all in the ternaries.
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