“…In addition, borates containing isolated B–O/F groups usually have metal cations with strong covalence (like M = Zn, Be, Al, etc. ), in which the cations with a higher valence state can form rigid chemical bonds (M–O/F) and break the anionic framework into a 0D configuration because of their stronger coordination ability. , Among them, the low polymerization degree of isolated B m –O/F ( m < 6) groups, like [BO 2 ], [BO 3 ], [BO 4 ], [B 2 O 5 ], [B 3 O 6 ], and [B 5 O 10 ] units, is much more than that of the highly polymerized ones (∼97 vs 3%). ,− To date, the [B 18 O 36 ] cluster is the largest one in the anhydrous borates and is found in Sr 8 MB 18 O 36 (M = Mg, Zn, Cd) , and NaSr 7 AlB 18 O 36 series . Other highly polymerized 0D clusters B m -O/F ( m ≥ 6), like [B 6 O n ] ( n = 12, 14), [B 7 O 14 ], [B 9 O 21 ], [B 11 O 22 ], [B 12 O 24 ] units, etc., are also very limited and have only been discovered in few borates. − Studies have shown that the highly polymerized B–O clusters tend to form the same and certain configurations, like [B 12 O 24 ] and [B 18 O 36 ] units, in related compounds and are all in a cyclic formation constructed by [B 3 O 7 ] and [B 3 O 8 ] branches with an end-to-end model, and both types show identical formulas and structures. − ,, Of course, the discovery of such borates greatly enriched the structural chemistry of the borate system.…”