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What are the downsides of creating one’s own string library?

What are the downsides of creating one’s own string library? Would it be better to use a platform-independent string?

A:

Speed is one of the big ones.
String objects in C# or Java typically have a lot of overhead; on a machine with a decent compiler, it’s rarely a problem (obviously it is at the limits of the machine, and for very large strings) but even on machines with less-efficient compilers it’s a good idea to minimize the number of C#/Java strings.
A large part of this is the fact that they typically allocate storage for them on the heap. In C#, you can get around this by using the StringBuilder class, but it’s still O(n) to access individual elements and O(1) to set or delete them – so, again, if you have a lot of strings, you probably want to minimize them.

2D, Pr–Ir Mixed-Valent Phosphonate Coordination Networks.
We report the synthesis, structural and magnetic characterizations, as well as electronic and optical properties of the mixed-valent phosphonates [Ph2PPr2(μ-O)2Ir2(μ-OH)2] (1, Pr-2) and [Ph2PPr2(μ-O)Ir2(μ-OH)2] (2, Ir-2). Compound 1 represents the first example of 2D coordination networks composed of a covalently bonded Pr phosphonate and an Ir phosphonate. The three-dimensional framework of 2D compound 2 features the first Pr-Ir mixed-valent coordination polymer in which Ir centers are bonded by two phosphonates and a coordinated water molecule. Magnetic measurements show that compounds 1 and 2 show magnetic features consistent with classical spin-1/2 models. Photochemical reactions of these molecules reveal that Ir centers are photochemically active, and photoinduced charge transfer (PT) processes between Pr and Ir centers are observed from photoinduced transient spectra. Reactions of the phosphonate ligands from the 2D compounds with nitric oxide (NO) show NO delivery to Pr and Ir centers, affording a 2D NO-based metal-organic framework structure.